ITGAM

gene
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Also known as HNA-4MAC-1CD11b

Summary

ITGAM (integrin subunit alpha M, HGNC:6149) is a protein-coding gene on chromosome 16p11.2, encoding Integrin alpha-M (P11215). Integrin ITGAM/ITGB2 is implicated in various adhesive interactions of monocytes, macrophages and granulocytes as well as in mediating the uptake of complement-coated particles and pathogens.

This gene encodes the integrin alpha M chain. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This I-domain containing alpha integrin combines with the beta 2 chain (ITGB2) to form a leukocyte-specific integrin referred to as macrophage receptor 1 (‘Mac-1’), or inactivated-C3b (iC3b) receptor 3 (‘CR3’). The alpha M beta 2 integrin is important in the adherence of neutrophils and monocytes to stimulated endothelium, and also in the phagocytosis of complement coated particles. Multiple transcript variants encoding different isoforms have been found for this gene.

Source: NCBI Gene 3684 — RefSeq curated summary.

At a glance

  • Gene–disease (curated): systemic lupus erythematosus (Supportive, GenCC)
  • GWAS associations: 24
  • Clinical variants (ClinVar): 1,126 total
  • Phenotypes (HPO): 44
  • Druggable target: yes
  • MANE Select transcript: NM_000632

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:6149
Approved symbolITGAM
Nameintegrin subunit alpha M
Location16p11.2
Locus typegene with protein product
StatusApproved
AliasesHNA-4, MAC-1, CD11b
Ensembl geneENSG00000169896
Ensembl biotypeprotein_coding
OMIM120980
Entrez3684

Gene structure

Transcript identifiers

Ensembl transcripts: 12 — 8 protein_coding, 4 retained_intron

ENST00000544665, ENST00000561838, ENST00000565142, ENST00000567031, ENST00000567178, ENST00000569746, ENST00000570242, ENST00000648685, ENST00000882543, ENST00000943359, ENST00000943360, ENST00000943361

RefSeq mRNA: 2 — MANE Select: NM_000632 NM_000632, NM_001145808

CCDS: CCDS45470, CCDS54004

Canonical transcript exons

ENST00000544665 — 30 exons

ExonStartEnd
ENSE000010288553126603031266147
ENSE000010288573127095431271084
ENSE000010288603132124131321371
ENSE000010288683132465131324782
ENSE000010289533127667131276744
ENSE000010289593127554931275699
ENSE000010289713127692031277049
ENSE000010289753127336531273518
ENSE000011918293133116531331275
ENSE000011918353133050431330605
ENSE000011918373133030831330421
ENSE000011918433133008131330164
ENSE000011918493132814731328230
ENSE000011918833132439931324553
ENSE000011918893132146431321627
ENSE000011919043127796731278109
ENSE000011919193127184731271992
ENSE000012421023132685631326935
ENSE000013048253126169231261797
ENSE000016756923126581131265881
ENSE000017091323129774531297954
ENSE000018025143126539531265498
ENSE000025972193133163631332877
ENSE000026071293125997531260092
ENSE000034830953132550031325622
ENSE000035521243132922831329303
ENSE000035567823132495831325031
ENSE000035737993132526331325404
ENSE000035946893129751431297654
ENSE000036347553132979831329905

Expression profiles

Bgee: expression breadth ubiquitous, 236 present calls, max score 98.90.

FANTOM5 (CAGE): breadth broad, TPM avg 16.8477 / max 994.4168, expressed in 493 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
15380112.0102483
1538024.0570353
1538000.6411138
2078430.139562

Top tissues by expression

280 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
monocyteCL:000057698.90gold quality
mononuclear cellCL:000084298.84gold quality
leukocyteCL:000073898.78gold quality
granulocyteCL:000009498.59gold quality
trabecular bone tissueUBERON:000248398.15gold quality
bone marrowUBERON:000237197.94gold quality
bloodUBERON:000017897.70gold quality
bone marrow cellCL:000209297.00gold quality
spleenUBERON:000210692.56gold quality
vermiform appendixUBERON:000115490.95gold quality
upper lobe of left lungUBERON:000895290.27gold quality
upper lobe of lungUBERON:000894889.92gold quality
deciduaUBERON:000245089.03gold quality
right lungUBERON:000216788.39gold quality
synovial jointUBERON:000221788.08gold quality
epithelium of nasopharynxUBERON:000195187.27gold quality
visceral pleuraUBERON:000240187.24gold quality
layer of synovial tissueUBERON:000761687.11gold quality
pleuraUBERON:000097787.10gold quality
lower lobe of lungUBERON:000894986.64gold quality
parietal pleuraUBERON:000240086.59gold quality
right coronary arteryUBERON:000162586.28gold quality
lungUBERON:000204885.87gold quality
omental fat padUBERON:001041485.57gold quality
peritoneumUBERON:000235885.48gold quality
superficial temporal arteryUBERON:000161485.45gold quality
adipose tissue of abdominal regionUBERON:000780885.38gold quality
caecumUBERON:000115385.02gold quality
C1 segment of cervical spinal cordUBERON:000646983.93gold quality
germinal epithelium of ovaryUBERON:000130483.66gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-ANND-3yes22.95
E-MTAB-9067yes13.49

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): CCL3, CD34, HIF1A, HNRNPK, IRF4, SP1, SPI1, STAT3, ZNF148

miRNA regulators (miRDB)

30 targeting ITGAM, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-6867-5P100.0082.213464
HSA-MIR-8485100.0077.574731
HSA-MIR-5692A100.0074.406850
HSA-MIR-3120-5P100.0065.56965
HSA-MIR-548AW99.9972.573559
HSA-MIR-548N99.9871.944170
HSA-MIR-6891-5P99.9866.531372
HSA-MIR-539-5P99.9370.302855
HSA-MIR-5010-3P99.8370.602357
HSA-MIR-451799.7669.191867
HSA-MIR-453099.6966.471509
HSA-MIR-7157-5P99.6669.331829
HSA-MIR-431099.5968.842527
HSA-MIR-464399.4967.631791
HSA-MIR-142-5P99.4870.922416
HSA-MIR-5590-3P99.4870.912429
HSA-MIR-806499.4566.92875
HSA-MIR-425199.4069.193363
HSA-MIR-377-3P99.3770.181905
HSA-MIR-7151-5P99.3767.82613
HSA-MIR-807099.0769.301303
HSA-MIR-6846-5P98.8165.861121
HSA-MIR-6848-5P98.8165.491126
HSA-MIR-60398.5868.281603
HSA-MIR-654-3P98.3867.61905
HSA-MIR-512-5P97.4766.48591
HSA-MIR-342-3P96.4467.481344
HSA-MIR-5579-5P96.3268.54730
HSA-MIR-1268A87.0661.46145
HSA-MIR-1268B87.0661.46145

Literature-anchored findings (GeneRIF, showing 40)

  • Mac-1 molecules mediated cell adhesion predominantly to fibrinogen, and its early degradation products, fragments X and Y (PMID:11881155)
  • CD11b-mediated adhesion of myeloid leukemia cells in the course of induced monocytic differentiation is crucial for cell attachment, development of a monocytic phenotype and subsequent survival. (PMID:11893077)
  • Respiratory syncytial virus enhances the expression of CD11b molecules by human eosinophils primed with platelet-activating factor (PMID:11937770)
  • CD11b may play an important role in pathogenic process(in COPD) (PMID:11953106)
  • fibroblasts prostaglandin-E2 is elevated in Alzheimer’s disease (prostaglandin-E2, PGE2) (PMID:12009501)
  • Identification of integrin alpha(M)beta(2) as an adhesion receptor on human peripheral blood monocytes for Cyr61 and connective tissue growth factor: immediate-early gene products expressed in atherosclerotic lesions.(integrin alpha(M)beta(2)) (PMID:12036876)
  • Impaired neutrophil actin assembly causes persistent expression and reduced primary granule exocytosis in Type II diabetes (PMID:12107753)
  • Increased expression of CD11b/CD18 adhesion molecules was obtained in PV and ET patients, which could be associated with increased leukocyte adehesiveness contributing to the hypercoagulable state. (PMID:12145463)
  • mediates type I phagocytosis under nonopsonic conditions and type II under opsonic conditions (PMID:12165526)
  • The junctional adhesion molecule 3 (JAM-3) on human platelets is a counterreceptor for the leukocyte integrin Mac-1. (PMID:12208882)
  • Histoplasma capsulatum inhibits apoptosis and Mac-1 expression in leucocytes. (PMID:12234260)
  • Mac-1 (CD11b) is required for neutrophil-Fc alpha RI binding of secretory IgA and subsequent neutrophil activation. (PMID:12244179)
  • investigation of molecular basis for broad ligand recognition (PMID:12377763)
  • iIgA promotes neutrophil apoptosis through a mechanism dependent on Mac-1(CD11b) cooperation, which involves the activation of the respiratory burst (PMID:12377937)
  • The mechanism that regulates the unmasking of the integrin alpha M cryptic binding site in the gamma C-domain of fibrinogen has been identified. (PMID:12390020)
  • recognition of uPA by alpha(M)beta(2) allows for formation of a multicontact trimolecular complex, in which a single uPA ligand may bind to both uPAR and alpha(M)beta(2); interaction of uPA with each receptor influences cell adhesion and migration (PMID:12393547)
  • ZBP-89 is a repressor of the human beta 2-integrin CD11b gene during differentiation of monocytes into macrophages (PMID:12393719)
  • The same lectin domain within CD11b regulates both the cytotoxic and adhesion functions of Mac-1/CR3. (PMID:12444150)
  • Stabilizing the integrin alpha M inserted domain in alternative conformations with a range of engineered disulfide bonds. (PMID:12466503)
  • Mac-1 (CD11b/CD18) is crucial for effective Fc receptor-mediated immunity to melanoma. (PMID:12485936)
  • Leptospira interrogans binds to the CR3 receptor on neutrophils (PMID:12495676)
  • Adhesion of dendritic cells derived from CD34+ progenitors to resting human dermal microvascular endothelial cells is down-regulated upon maturation and partially depends on CD11a-CD18, CD11b-CD18 and CD36. (PMID:12516552)
  • Level of expression of the adhesion molecule/complement receptor CD11b/CD18 and the chemokine receptor IL-8 receptor-A was also higher after vaginal delivery. (PMID:12576754)
  • the expression of ICAM-1 might involve both p38 MAPK and NF-kappaB activities, whereas the regulation of CD11b, CD18, and ICAM-3 expressions might be mediated through p38 MAPK but not NF-kappaB. (PMID:12600815)
  • uPAR up-regulated the Mac-1 adhesion to fibrinogen, and focal adhesion kinase and MAPK were involved in this regulation (PMID:12665127)
  • ICAM-4 binds to the I domain of this integrin. (PMID:12694184)
  • Fibrinogen-CD11b/CD18 interaction activates the NF-kappa B pathway and delays apoptosis in human neutrophils. (PMID:12731070)
  • Our results indicate that induction of Ca2+ entry by the depletion of Ca2+ from intracellular stores upregulates CD11b/CD18 expression on eosinophils and primes eosinophil transmigration across lung epithelium. (PMID:12760968)
  • three separate domains of alpha M beta 2 (the alpha MI-domain, the alpha M beta-propeller, and the beta 2I-domain) function together and contribute to the formation of the C3bi-binding site (PMID:12816955)
  • The extracellular, membrane-proximal region of the CD11b receptor subunit plays an important role in integrin activation and therefore could be targeted by certain cell surface proteins as a conduit to control the integrin “inside-out” signaling process. (PMID:12847278)
  • Interaction of proteinase 3 with CD11b/CD18 (beta2 integrin) on the cell membrane of human neutrophils. (PMID:12960243)
  • cooperative engagement of CR3 on both the lectin-like site involved in beta-glucan binding and the I-domain involved in C3bi binding produces AA release (PMID:14532278)
  • CD11b expression with the whole blood flow cytometry seemed feasible and reliable in the early diagnosis of neonatal sepsis. (PMID:14751053)
  • assembly of Plg and uPA on integrin alpha(M)beta(2) regulates Plm activity and plays a crucial role in neutrophil-mediated thrombolysis (PMID:14769799)
  • The interaction between Mac-1 and Thy-1 is involved in the adhesion of leukocytes to activated endothelial cells as well as in subsequent transendothelial migration of leukocytes into the perivascular tissue. (PMID:15004192)
  • Some anti-Mart antibodies interfere with Mac-1-dependent cellular functions of neutrophils. (PMID:15073035)
  • platelet-activating factor or interleukin 8 acted in concert with P-selectin for further enhancing the activation of alphaMbeta2 (PMID:15217824)
  • Myeloid-related proteins-induced increased adhesion of monocytes to Fibronectin and upregulation of CD11b contribute to a facilitated accumulation of monocytes (PMID:15277376)
  • BAP31 may play a role in regulating intracellular trafficking of CD11b/CD18 in neutrophils (PMID:15294914)
  • studies of the interaction of the ligand binding alphaMI-domain of alphaMbeta2 with the D fragment of fibrinogen, which has multiple binding sites for integrin alphaMbeta2 (PMID:15304494)

Cross-species orthologs

9 orthologs

OrganismSymbolGene ID
mus_musculusItgamENSMUSG00000030786
rattus_norvegicusItgadENSRNOG00000019728
drosophila_melanogasterifFBGN0001250
drosophila_melanogastermewFBGN0004456
drosophila_melanogasterItgaPS4FBGN0034005
drosophila_melanogasterItgaPS5FBGN0034880
drosophila_melanogasterscbFBGN0286785
caenorhabditis_elegansWBGENE00002081
caenorhabditis_elegansWBGENE00003929

Paralogs (17): ITGAL (ENSG00000005844), ITGA3 (ENSG00000005884), ITGA2B (ENSG00000005961), ITGA8 (ENSG00000077943), ITGAE (ENSG00000083457), ITGA6 (ENSG00000091409), ITGA4 (ENSG00000115232), ITGA7 (ENSG00000135424), ITGA11 (ENSG00000137809), ITGAV (ENSG00000138448), ITGAX (ENSG00000140678), ITGA10 (ENSG00000143127), ITGA9 (ENSG00000144668), ITGAD (ENSG00000156886), ITGA5 (ENSG00000161638), ITGA2 (ENSG00000164171), ITGA1 (ENSG00000213949)

Protein

Protein identifiers

Integrin alpha-MP11215 (reviewed: P11215)

Alternative names: CD11 antigen-like family member B, CR-3 alpha chain, Cell surface glycoprotein MAC-1 subunit alpha, Leukocyte adhesion receptor MO1, Neutrophil adherence receptor

All UniProt accessions (3): P11215, H3BMV4, I3NI33

UniProt curated annotations — full annotation on UniProt →

Function. Integrin ITGAM/ITGB2 is implicated in various adhesive interactions of monocytes, macrophages and granulocytes as well as in mediating the uptake of complement-coated particles and pathogens. It is identical with CR-3, the receptor for the iC3b fragment of the third complement component. It probably recognizes the R-G-D peptide in C3b. Integrin ITGAM/ITGB2 is also a receptor for fibrinogen and factor X. It recognizes P1 and P2 peptides of fibrinogen gamma chain. Regulates neutrophil migration. In association with beta subunit ITGB2/CD18, required for CD177-PRTN3-mediated activation of TNF primed neutrophils. Integrin ITGAM/ITGB2 is also a receptor for ICAM1 ligand ensuring adhesion between stimulated neutrophils and stimulated endothelial cells. May regulate phagocytosis-induced apoptosis in extravasated neutrophils. May play a role in mast cell development. Required with TYROBP/DAP12 in microglia to control production of microglial superoxide ions which promote the neuronal apoptosis that occurs during brain development.

Subunit / interactions. Heterodimer of an alpha and a beta subunit. ITGAM associates with ITGB2. Found in a complex with CD177 and ITGB2/CD18. Interacts with JAM3. Interacts with THBD. Interacts with complement factor H/CFH; this interaction mediates adhesion of neutrophils to pathogens leading to pathogen clearance. Interacts with TMEM268; this interaction inhibits ITGAM degradation via the endosome-lysosome pathway.

Subcellular location. Cell membrane. Membrane raft.

Tissue specificity. Predominantly expressed in monocytes and granulocytes. Expressed in neutrophils (at protein level).

Disease relevance. Systemic lupus erythematosus 6 (SLEB6) [MIM:609939] A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. Disease susceptibility may be associated with variants affecting the gene represented in this entry.

Domain organisation. The integrin I-domain (insert) is a VWFA domain. Integrins with I-domains do not undergo protease cleavage.

Similarity. Belongs to the integrin alpha chain family.

Isoforms (2)

UniProt IDNamesCanonical?
P11215-11yes
P11215-22

RefSeq proteins (2): NP_000623, NP_001139280 (=MANE)

Domains & families (InterPro)

IDNameType
IPR000413Integrin_alphaFamily
IPR002035VWF_ADomain
IPR013517FG-GAPRepeat
IPR013519Int_alpha_beta-pRepeat
IPR013649Integrin_alpha_Ig-like_1Domain
IPR018184Integrin_alpha_C_CSConserved_site
IPR028994Integrin_alpha_NHomologous_superfamily
IPR032695Integrin_dom_sfHomologous_superfamily
IPR036465vWFA_dom_sfHomologous_superfamily
IPR048285Integrin_alpha_Ig-like_2Domain
IPR048633ITGAX-like_Ig_3Domain

Pfam: PF00092, PF00357, PF01839, PF08441, PF20805, PF21520

UniProt features (170 total): strand 77, helix 22, glycosylation site 19, turn 11, binding site 11, disulfide bond 10, repeat 7, sequence variant 4, topological domain 2, signal peptide 1, chain 1, short sequence motif 1, transmembrane region 1, splice variant 1, sequence conflict 1, domain 1

Structure

Experimental structures (PDB)

31 structures, top 30 by resolution.

PDBMethodResolution (Å)
1MF7X-RAY DIFFRACTION1.25
1NA5X-RAY DIFFRACTION1.5
8CE6X-RAY DIFFRACTION1.58
1IDOX-RAY DIFFRACTION1.7
1JLMX-RAY DIFFRACTION2
4XW2X-RAY DIFFRACTION2
8CE9X-RAY DIFFRACTION2.11
1M1UX-RAY DIFFRACTION2.3
1N9ZX-RAY DIFFRACTION2.5
9RM9ELECTRON MICROSCOPY2.6
1BHOX-RAY DIFFRACTION2.7
1BHQX-RAY DIFFRACTION2.7
1IDNX-RAY DIFFRACTION2.7
3Q3GX-RAY DIFFRACTION2.7
7USLELECTRON MICROSCOPY2.7
7USMELECTRON MICROSCOPY2.7
9T5WELECTRON MICROSCOPY2.74
6RHWX-RAY DIFFRACTION2.75
4M76X-RAY DIFFRACTION2.8
3QA3X-RAY DIFFRACTION3
9T5VELECTRON MICROSCOPY3.06
9T5ZELECTRON MICROSCOPY3.1
7P2DX-RAY DIFFRACTION3.2
7AKKX-RAY DIFFRACTION3.4
9T3YELECTRON MICROSCOPY3.44
9GMUX-RAY DIFFRACTION3.8
9RMAELECTRON MICROSCOPY3.94
2LKESOLUTION NMR
2LKJSOLUTION NMR
8VOHSOLUTION NMR

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P11215-F186.300.51

Antibody-complex structures (SAbDab): 53Q3G, 3QA3, 7P2D, 7USL, 9GMU

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Ligand- & substrate-binding residues (11): 465; 467; 469; 473; 529; 531; 533; 537; 592; 596; 600

Disulfide bonds (10): 66–73, 105–123, 113–144, 494–505, 638–721, 654–711, 770–776, 847–864, 998–1022, 1027–1032

Glycosylation sites (19): 86, 240, 391, 469, 692, 696, 734, 801, 880, 900, 911, 940, 946, 978, 993, 1021, 1044, 1050, 1075

Function

Pathways and Gene Ontology

Reactome pathways

12 pathways

IDPathway
R-HSA-166016Toll Like Receptor 4 (TLR4) Cascade
R-HSA-202733Cell surface interactions at the vascular wall
R-HSA-216083Integrin cell surface interactions
R-HSA-6785807Interleukin-4 and Interleukin-13 signaling
R-HSA-6798695Neutrophil degranulation
R-HSA-109582Hemostasis
R-HSA-1280215Cytokine Signaling in Immune system
R-HSA-1474244Extracellular matrix organization
R-HSA-168249Innate Immune System
R-HSA-168256Immune System
R-HSA-168898Toll-like Receptor Cascades
R-HSA-449147Signaling by Interleukins

MSigDB gene sets: 474 (showing top): GOBP_PHENOL_CONTAINING_COMPOUND_METABOLIC_PROCESS, GOBP_RESPONSE_TO_NITROGEN_COMPOUND, REACTOME_INNATE_IMMUNE_SYSTEM, GOBP_RESPONSE_TO_ESTRADIOL, GOBP_RESPONSE_TO_AMINE, SWEET_KRAS_ONCOGENIC_SIGNATURE, REACTOME_CYTOKINE_SIGNALING_IN_IMMUNE_SYSTEM, MODULE_255, GOBP_INFLAMMATORY_RESPONSE, GOCC_SECRETORY_GRANULE, GOBP_POSITIVE_REGULATION_OF_LEUKOCYTE_DEGRANULATION, MODULE_45, MODULE_64, GOBP_REGULATION_OF_SUPEROXIDE_ANION_GENERATION, GOBP_PROTEIN_TARGETING

GO Biological Process (29): microglial cell activation (GO:0001774), response to amphetamine (GO:0001975), complement receptor mediated signaling pathway (GO:0002430), response to ischemia (GO:0002931), receptor-mediated endocytosis (GO:0006898), phagocytosis, engulfment (GO:0006911), cell adhesion (GO:0007155), cell-matrix adhesion (GO:0007160), integrin-mediated signaling pathway (GO:0007229), response to mechanical stimulus (GO:0009612), ectodermal cell differentiation (GO:0010668), forebrain development (GO:0030900), response to estradiol (GO:0032355), positive regulation of superoxide anion generation (GO:0032930), heterotypic cell-cell adhesion (GO:0034113), positive regulation of neutrophil degranulation (GO:0043315), innate immune response (GO:0045087), negative regulation of dopamine metabolic process (GO:0045963), positive regulation of protein targeting to membrane (GO:0090314), amyloid-beta clearance (GO:0097242), cell-cell adhesion (GO:0098609), obsolete cell-cell adhesion via plasma-membrane adhesion molecules (GO:0098742), response to Gram-positive bacterium (GO:0140459), complement-mediated synapse pruning (GO:0150062), vertebrate eye-specific patterning (GO:0150064), positive regulation of microglial cell mediated cytotoxicity (GO:1904151), response to curcumin (GO:1904643), immune system process (GO:0002376), positive regulation of metabolic process (GO:0009893)

GO Molecular Function (9): amyloid-beta binding (GO:0001540), complement component C3b binding (GO:0001851), integrin binding (GO:0005178), heat shock protein binding (GO:0031072), signaling receptor activity (GO:0038023), cargo receptor activity (GO:0038024), metal ion binding (GO:0046872), protein binding (GO:0005515), protein-containing complex binding (GO:0044877)

GO Cellular Component (12): obsolete extracellular space (GO:0005615), plasma membrane (GO:0005886), integrin complex (GO:0008305), external side of plasma membrane (GO:0009897), cell surface (GO:0009986), integrin alphaM-beta2 complex (GO:0034688), specific granule membrane (GO:0035579), plasma membrane raft (GO:0044853), extracellular exosome (GO:0070062), tertiary granule membrane (GO:0070821), membrane (GO:0016020), membrane raft (GO:0045121)

Reactome top-level categories

Rollup of top-7 pathways:

CategoryPathways
Innate Immune System2
Immune System2
Toll-like Receptor Cascades1
Hemostasis1
Extracellular matrix organization1
Signaling by Interleukins1
Cytokine Signaling in Immune system1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding2
plasma membrane2
cellular anatomical structure2
secretory granule membrane2
leukocyte activation involved in inflammatory response1
macrophage activation1
glial cell activation1
response to amine1
immune response-activating cell surface receptor signaling pathway1
response to stress1
endocytosis1
phagocytosis1
plasma membrane invagination1
cellular process1
cell-substrate adhesion1
cell surface receptor signaling pathway1
response to external stimulus1
response to abiotic stimulus1
ectoderm development1
cell differentiation1
brain development1
anatomical structure development1
response to lipid1
response to oxygen-containing compound1
regulation of superoxide anion generation1
superoxide anion generation1
positive regulation of reactive oxygen species metabolic process1
cell-cell adhesion1
positive regulation of myeloid leukocyte mediated immunity1
positive regulation of leukocyte degranulation1
neutrophil degranulation1
regulation of neutrophil degranulation1
positive regulation of immune response1
immune response1
defense response to symbiont1
negative regulation of amine metabolic process1
regulation of dopamine metabolic process1
dopamine metabolic process1
protein targeting to membrane1
positive regulation of cellular process1

Protein interactions and networks

STRING

4626 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ITGAMITGB2P05107999
ITGAMICAM1P05362996
ITGAMTHY1P04216987
ITGAMVCAM1P19320986
ITGAMGP1BAP07359982
ITGAMICAM2P13598968
ITGAMCD209Q9NNX6960
ITGAMPTPRCP08575955
ITGAMFCGR3BO75015947
ITGAMJAM3Q9BX67940
ITGAMCD8AP01732932
ITGAMITGALP20701930
ITGAMCD4P01730929
ITGAMSELPP16109926
ITGAMMRC1P22897924

IntAct

124 interactions, top by confidence:

ABTypeScore
ITGAMPTNpsi-mi:“MI:0407”(direct interaction)0.620
ITGAMTMX2psi-mi:“MI:0915”(physical association)0.560
ITGAMHSD17B13psi-mi:“MI:0915”(physical association)0.560
ITGAMPIGPpsi-mi:“MI:0915”(physical association)0.560
ITGAMTMEM14Bpsi-mi:“MI:0915”(physical association)0.560
ITGAMABHD16Apsi-mi:“MI:0915”(physical association)0.560
ITGAMKASH5psi-mi:“MI:0915”(physical association)0.560
ITGAMpsi-mi:“MI:0915”(physical association)0.560
ITGAMCREB3L1psi-mi:“MI:0915”(physical association)0.560
GPR42ITGAMpsi-mi:“MI:0915”(physical association)0.560
ITGAMMRM1psi-mi:“MI:0915”(physical association)0.560
ITGAMREEP2psi-mi:“MI:0915”(physical association)0.560
ITGAMSLC10A6psi-mi:“MI:0915”(physical association)0.560
ITGAMCD79Apsi-mi:“MI:0915”(physical association)0.560
ITGAMKCNJ6psi-mi:“MI:0915”(physical association)0.560
ITGAMKIR2DL3psi-mi:“MI:0915”(physical association)0.560
ITGAMGJA8psi-mi:“MI:0915”(physical association)0.560
ITGAMTMEM52Bpsi-mi:“MI:0915”(physical association)0.560
ITGAMELOVL4psi-mi:“MI:0915”(physical association)0.560
ITGAMCERS4psi-mi:“MI:0915”(physical association)0.560
ITGAMSYT2psi-mi:“MI:0915”(physical association)0.560
GJB1ITGAMpsi-mi:“MI:0915”(physical association)0.560
ITGAMRUSF1psi-mi:“MI:0915”(physical association)0.560
ITGAMGORABpsi-mi:“MI:0915”(physical association)0.560

BioGRID (66): SHARPIN (Protein-peptide), ITGAM (Co-fractionation), ITGAM (Two-hybrid), ITGAM (Affinity Capture-Western), ITGAM (Affinity Capture-MS), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid), ITGAM (Two-hybrid)

ESM2 similar proteins: A2ARA8, B0S5N4, B8JK39, F1MMS9, O08665, P05555, P06756, P08514, P08648, P11215, P11688, P13612, P17301, P17852, P18564, P20701, P23229, P24063, P26006, P26007, P26008, P26009, P38570, P43406, P53708, P53710, P53711, P61622, P61625, P80746, Q00651, Q06274, Q13683, Q13797, Q60677, Q61738, Q61739, Q62469, Q62470, Q63258

Diamond homologs: A2AX52, A6H584, A6NMZ7, A6QLN9, A8TX70, E7FF10, O00339, O08746, O42401, O75578, O89029, P05099, P05555, P11215, P12111, P15989, P20701, P20702, P34576, P51942, P61625, Q02388, Q13349, Q21281, Q21540, Q28902, Q3V0T4, Q63870, Q642A6, Q6PCB0, Q6UXI7, Q8C6K9, Q8NFW1, Q8R2Z5, Q90615, Q91145, Q923P0, Q95LI2, Q96P44, Q9P218

SIGNOR signaling

6 interactions.

AEffectBMechanism
ITGAMup-regulatesICAM1binding
SPI1“up-regulates quantity by expression”ITGAM“transcriptional regulation”
ITGAMup-regulatesDifferentiation
ITGAM“form complex”“AM/b2 integrin”binding
C5AR2“up-regulates quantity by expression”ITGAM
C5AR1“up-regulates quantity by expression”ITGAM

Disease & clinical

Clinical variants and AI predictions

ClinVar

1126 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance633
Likely benign434
Benign30

Top pathogenic / likely-pathogenic (0)

SpliceAI

4194 predictions. Top by Δscore:

VariantEffectΔscore
16:31265391:ACAG:Aacceptor_gain1.0000
16:31265393:AG:Aacceptor_gain1.0000
16:31265393:AGGGT:Aacceptor_gain1.0000
16:31265394:GG:Gacceptor_gain1.0000
16:31265394:GGGTG:Gacceptor_gain1.0000
16:31265494:GCAGG:Gdonor_gain1.0000
16:31265495:CAGGG:Cdonor_loss1.0000
16:31265496:AGGG:Adonor_loss1.0000
16:31265497:GG:Gdonor_gain1.0000
16:31265497:GGGTG:Gdonor_loss1.0000
16:31265498:GG:Gdonor_gain1.0000
16:31265499:G:GGdonor_gain1.0000
16:31265809:A:AGacceptor_gain1.0000
16:31265810:G:GAacceptor_gain1.0000
16:31270949:CCCA:Cacceptor_loss1.0000
16:31270951:CAG:Cacceptor_loss1.0000
16:31270952:A:AGacceptor_gain1.0000
16:31270952:A:ATacceptor_loss1.0000
16:31270952:AG:Aacceptor_gain1.0000
16:31270953:G:GAacceptor_loss1.0000
16:31270953:G:GGacceptor_gain1.0000
16:31270953:GG:Gacceptor_gain1.0000
16:31270953:GGGT:Gacceptor_gain1.0000
16:31271096:GGG:Gdonor_gain1.0000
16:31271097:GGG:Gdonor_gain1.0000
16:31271988:GTGGT:Gdonor_gain1.0000
16:31273351:T:Aacceptor_gain1.0000
16:31273358:T:Aacceptor_gain1.0000
16:31273360:CACA:Cacceptor_loss1.0000
16:31273361:A:AGacceptor_gain1.0000

AlphaMissense

7553 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:31330531:A:CS1068R0.996
16:31330533:C:AS1068R0.996
16:31330533:C:GS1068R0.996
16:31271040:T:CF172L0.992
16:31271042:T:AF172L0.992
16:31271042:T:GF172L0.992
16:31270994:T:AD156E0.990
16:31270994:T:GD156E0.990
16:31270993:A:TD156V0.989
16:31270999:C:TS158F0.989
16:31273434:T:AD258E0.989
16:31273434:T:GD258E0.989
16:31331222:A:CS1112R0.989
16:31331224:C:AS1112R0.989
16:31331224:C:GS1112R0.989
16:31271004:A:CS160R0.988
16:31271006:C:AS160R0.988
16:31271006:C:GS160R0.988
16:31273433:A:TD258V0.988
16:31275642:T:CF318L0.988
16:31275644:T:AF318L0.988
16:31275644:T:GF318L0.988
16:31270984:T:CF153S0.987
16:31270998:T:CS158P0.987
16:31271865:T:CS193P0.987
16:31275643:T:GF318C0.986
16:31261763:T:CF34L0.985
16:31261765:C:AF34L0.985
16:31261765:C:GF34L0.985
16:31275601:C:AA304E0.985

dbSNP variants (sampled 300 via entrez): RS1000068561 (16:31284488 C>T), RS1000069240 (16:31261515 T>G), RS1000120561 (16:31305458 G>A), RS1000131278 (16:31312027 TCGCAAGGACAAAAAACCA>T), RS1000146715 (16:31267197 T>C), RS1000167555 (16:31273851 T>A), RS1000186565 (16:31323600 T>C), RS1000187394 (16:31280319 A>C,G), RS1000211536 (16:31286298 G>A), RS1000215114 (16:31323470 G>C), RS1000261333 (16:31307348 C>G), RS1000278079 (16:31329767 C>T), RS1000315956 (16:31285641 A>T), RS1000325698 (16:31285964 G>A,T), RS1000394651 (16:31329484 C>A,T)

Disease associations

OMIM: gene MIM:120980 | disease phenotypes:

GenCC curated gene-disease

DiseaseClassificationInheritance
systemic lupus erythematosusSupportiveUnknown

Mondo (1): systemic lupus erythematosus (MONDO:0007915)

Orphanet (0):

HPO phenotypes

44 total (30 of 44 shown, HPO-id order):

HPOTerm
HP:0000093Proteinuria
HP:0000155Oral ulcer
HP:0000488Retinopathy
HP:0000716Depression
HP:0000790Hematuria
HP:0000822Hypertension
HP:0000992Cutaneous photosensitivity
HP:0001250Seizure
HP:0001369Arthritis
HP:0001596Alopecia
HP:0001824Weight loss
HP:0001873Thrombocytopenia
HP:0001878Hemolytic anemia
HP:0001882Decreased total leukocyte count
HP:0001945Fever
HP:0002039Anorexia
HP:0002072Chorea
HP:0002716Lymphadenopathy
HP:0003453Antineutrophil antibody positivity
HP:0003493Antinuclear antibody positivity
HP:0005421Decreased circulating complement C3 concentration
HP:0005764Polyarticular arthritis
HP:0007417Discoid lupus rash
HP:0012085Pyuria
HP:0012378Fatigue
HP:0020151Anti-dsDNA antibody positivity
HP:0025300Malar rash
HP:0030880Raynaud phenomenon
HP:0032235Anti-La/SS-B antibody positivity
HP:0033028Anti-U1 ribonucleoprotein antibody positivity

GWAS associations

24 associations (top):

StudyTraitp-value
GCST000142_4Systemic lupus erythematosus2.000000e-23
GCST000144_6Systemic lupus erythematosus3.000000e-11
GCST000216_5Systemic lupus erythematosus2.000000e-06
GCST000996_16Systemic lupus erythematosus1.000000e-15
GCST001795_34Systemic lupus erythematosus7.000000e-06
GCST002069_18Systemic lupus erythematosus and Systemic sclerosis1.000000e-10
GCST002463_22Systemic lupus erythematosus4.000000e-11
GCST002655_1IgA nephropathy1.000000e-08
GCST002655_10IgA nephropathy8.000000e-13
GCST002655_9IgA nephropathy1.000000e-11
GCST003155_20Systemic lupus erythematosus3.000000e-76
GCST003156_18Systemic lupus erythematosus4.000000e-53
GCST003252_5Systemic lupus erythematosus3.000000e-21
GCST003622_41Systemic lupus erythematosus5.000000e-48
GCST004867_36Systemic lupus erythematosus2.000000e-20
GCST005524_8Autoimmune thyroid diseases (Graves disease or Hashimoto’s thyroiditis)5.000000e-08
GCST005526_8Graves’ disease4.000000e-08
GCST005752_124Systemic lupus erythematosus9.000000e-85
GCST005752_20Systemic lupus erythematosus7.000000e-22
GCST005752_24Systemic lupus erythematosus2.000000e-13
GCST007400_40Systemic lupus erythematosus3.000000e-62
GCST009240_34Serum metabolite levels (CMS)6.000000e-11
GCST010241_223Apolipoprotein A1 levels2.000000e-09
GCST011426_34Systemic lupus erythematosus6.000000e-08

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004614apolipoprotein A 1 measurement

MeSH disease descriptors (1)

DescriptorNameTree numbers
D008180Lupus Erythematosus, SystemicC17.300.480; C20.111.590

Drugs & pharmacology

Drug and pharmacology data

Is drug target: yes

ChEMBL targets (3): CHEMBL2111362 (PROTEIN COMPLEX), CHEMBL3826 (SINGLE PROTEIN), CHEMBL4106121 (PROTEIN-PROTEIN INTERACTION)

PharmGKB: 1 entry (VIP=true, CPIC=false)

GtoPdb / IUPHAR curated pharmacology

(IUPHAR/BPS Guide to Pharmacology — expert-curated)

Target class: catalytic receptor — Integrins

ChEMBL bioactivities

9 potent at pChembl≥5 of 20 total, top 9 by pChembl (potency: 10 = 0.1 nM, 6 = 1 µM).

pChemblTypeValueUnitMolecule
7.33IC5047.2nMCHEMBL5417237
7.27IC5053.4nMCHEMBL5417237
6.85IC50140nMCHEMBL4243248
6.61IC50244nMCHEMBL5419935
6.48IC50330nMCHEMBL81782
6.45IC50353nMCHEMBL5419935
5.60IC502500nMCHEMBL81782
5.60IC502500nMCHEMBL4243248
5.19IC506500nMCHEMBL5271349

PubChem BioAssay actives

9 with measured affinity, of 57 total; 5 most potent distinct compounds. Largely complementary to BindingDB; screening values are coarse (µM, 4 dp), so sub-nM hits tie at the floor.

CompoundAssayTypeValueUnit
(2S,5S,8S,11S,14S)-8-methyl-2-[[4-[(2-methylphenyl)carbamoylamino]phenyl]methyl]-5-(2-methylpropyl)-3,6,9,12,16-pentaoxo-11-propan-2-yl-1,4,7,10,13-pentazacyclohexadecane-14-carboxylic acid2029965: Binding affinity to alphaMbeta2 integrin receptor (unknown origin) preincubated for 30 mins followed by 30 mins incubation in fibrinogen coated wells by fluorescence based assayic500.0472uM
2-[(1E,3E)-4-(3,4-dihydro-2H-quinolin-1-yl)buta-1,3-dienyl]-1-ethylbenzo[e][1,3]benzothiazol-1-ium chloride1393264: Inhibition of C3bi-AP binding to CR3 derived from human PMNic500.1400uM
(2R,5S,8S,11S,14R)-8-(carboxymethyl)-2-[[4-[(2-methylphenyl)carbamoylamino]phenyl]methyl]-5-(2-methylpropyl)-3,6,9,12,16-pentaoxo-11-propan-2-yl-1,4,7,10,13-pentazacyclohexadecane-14-carboxylic acid2029965: Binding affinity to alphaMbeta2 integrin receptor (unknown origin) preincubated for 30 mins followed by 30 mins incubation in fibrinogen coated wells by fluorescence based assayic500.2440uM
(2E)-3-ethyl-2-[(Z)-3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)prop-2-enylidene]-1,3-benzothiazole iodide1393264: Inhibition of C3bi-AP binding to CR3 derived from human PMNic500.3300uM
(3S)-3-[[2-[[(2S)-2-[[(1R,3R,4aS,4bS,6aS,8S,10aS,10bS,12aS)-8-methoxy-10a,12a-dimethylspiro[3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-tetradecahydronaphtho[2,1-f]isochromene-1,2’-oxolane]-3-carbonyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]acetyl]amino]-4-amino-4-oxobutanoic acid1927075: Antagonist activity at integrin CD11B/CD18 (unknown origin)ic506.5000uM

CTD chemical–gene interactions

160 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Tretinoindecreases reaction, increases expression, increases localization, affects expression, increases response to substance (+5 more)39
Tetradecanoylphorbol Acetatedecreases reaction, increases expression, increases localization, affects cotreatment12
Calcitriolaffects cotreatment, increases expression, increases reaction, affects binding, decreases reaction11
Arsenic Trioxidedecreases expression, decreases reaction, increases expression, increases reaction, affects cotreatment9
2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-onedecreases reaction, increases expression, increases reaction, affects cotreatment, decreases expression5
Dimethyl Sulfoxideaffects cotreatment, decreases reaction, increases expression, increases reaction5
N-Formylmethionine Leucyl-Phenylalaninedecreases reaction, increases expression, increases reaction5
tamibarotenedecreases reaction, increases expression, affects expression, increases reaction4
3-methyladenineaffects localization, increases localization, affects cotreatment, decreases reaction, increases expression3
2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-onedecreases reaction, increases expression3
U 0126affects cotreatment, decreases reaction, increases expression3
lithocholic acid acetateaffects cotreatment, increases expression3
Calcimycinaffects cotreatment, increases expression, decreases reaction3
Decitabineaffects expression, increases expression, increases reaction3
Lipopolysaccharidesincreases expression3
sodium arseniteincreases expression2
arsenic disulfidedecreases reaction, increases expression, increases reaction2
4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazoledecreases reaction, increases expression, increases reaction2
4-amino-2-trifluoromethyl-phenyl retinatedecreases reaction, increases expression, affects expression, increases reaction2
Cadmiumaffects cotreatment, increases expression, decreases reaction, decreases expression, increases abundance2
Dexamethasonedecreases reaction, increases expression, increases reaction2
Heparindecreases expression, increases expression2
Platelet Activating Factordecreases reaction, increases expression, increases reaction2
Vitamin Dincreases expression, increases reaction2
Cadmium Chloridedecreases expression, increases abundance, increases expression2
Sirolimusaffects cotreatment, decreases reaction, increases expression, increases localization, increases reaction2
aristolochic acid Iincreases expression1
SHP099increases expression, increases reaction1
4-(2-aminoethyl)benzenesulfonylfluoridedecreases reaction, increases localization1
parthenolideincreases expression, increases reaction1

ChEMBL screening assays

14 unique, capped per target: 12 binding, 2 functional

Representative assays (with source publication via chembl_document):

Assay IDTypeDescriptionSource paper
CHEMBL1037931FunctionalAgonist activity at CD11b/CD18 expressed in K562 cells assessed as increase in cell adhesion to fibrinogenIdentification of novel agonists of the integrin CD11b/CD18. — Bioorg Med Chem Lett
CHEMBL1249611BindingBinding affinity to alphaMbeta2 integrin expressed in CHO cells by flow cytometryCombinatorial chemistry identifies high-affinity peptidomimetics against alpha4beta1 integrin for in vivo tumor imaging. — Nat Chem Biol

Cellosaurus cell lines

7 cell lines: 6 cancer cell line, 1 transformed cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_B8ITAbcam HCT 116 ITGAM KOCancer cell lineMale
CVCL_B8XNAbcam MCF-7 ITGAM KOCancer cell lineFemale
CVCL_B9L3Abcam A-549 ITGAM KOCancer cell lineMale
CVCL_D7SPUbigene A-549 ITGAM KOCancer cell lineMale
CVCL_D8EJUbigene BEAS-2B ITGAM KOTransformed cell lineMale
CVCL_E4AHK-562 KC/16Cancer cell lineFemale
CVCL_F1U5HyCyte THP-1 KO-hITGAMCancer cell lineMale

Clinical trials (associated diseases)

300 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT00120887PHASE4COMPLETEDLupus Atherosclerosis Prevention Study
NCT00125307PHASE4COMPLETEDTacrolimus for the Treatment of Systemic Lupus Erythematosus With Membranous Nephritis
NCT00188188PHASE4UNKNOWNStudy of Endothelial Dysfunction in Systemic Lupus and Its Role in Heart Disease
NCT00371501PHASE4COMPLETEDAspirin and Statins for Prevention of Atherosclerosis and Arterial Thromboembolism in Systemic Lupus Erythematosus
NCT00392093PHASE4COMPLETEDEffect of Hormone Replacement Therapy on Lupus Activity
NCT00413361PHASE4COMPLETEDThe Reduction of Systemic Lupus Erythematosus Flares :Study PLUS
NCT00508898PHASE4WITHDRAWNThe Efficacy and Safety of Calcitriol for the Treatment of Lupus Nephritis and Persistent Proteinuria
NCT00668330PHASE4COMPLETEDSteroid Induced Osteoporosis in Patients With Systemic Lupus Erythematosus
NCT00739050PHASE4TERMINATEDEffect of Simvastatin on Endothelial Function in Premenopausal Women With Systemic Lupus Erythematosus (0733-271)(TERMINATED)
NCT00815282PHASE4COMPLETEDImmune Response After Human Papillomavirus Vaccination in Patients With Autoimmune Disease
NCT00828178PHASE4COMPLETEDEfficacy of Fish Oil in Lupus Patients
NCT00866229PHASE4UNKNOWNEfficacy and Adverse Effect of Simvastatin Compare to Rosuvastatin in Systemic Lupus Erythematosus (SLE) Patients With Corticosteroid Therapy and High Low-Density Lipoprotein (LDL) Cholesterol Level
NCT00911521PHASE4COMPLETEDImmunogenicity and Safety of a Quadrivalent Human Papillomavirus (HPV) Vaccine in Patients With SLE: a Controlled Study
NCT01101802PHASE4COMPLETEDMycophenolate Mofetil in Systemic Lupus Erythematosus (MISSILE)
NCT01112215PHASE4COMPLETEDEnteric-coated Mycophenolate Sodium Versus Azathioprine for the Extra-renal Lupus Manifestations
NCT01151644PHASE4UNKNOWNSafety and Efficacy of Anti-Pandemic H1N1 Vaccination in Rheumatic Diseases
NCT01276782PHASE4WITHDRAWNLevothyroxine in Pregnant SLE Patients
NCT01322308PHASE4COMPLETEDEffect of Pioglitazone on Endothelial Function in Premenopausal Women With Uncomplicated Systemic Lupus Erythematosus
NCT01359826PHASE4WITHDRAWNThe Effect of Milnacipran on Fatigue and Quality of Life in Lupus Patients
NCT01597492PHASE4COMPLETEDA Study to Evaluate the Effect of Belimumab on Vaccine Responses in Subjects With Systemic Lupus Erythematosus (SLE)
NCT01632241PHASE4COMPLETEDEfficacy and Safety of Belimumab in Black Race Patients With Systemic Lupus Erythematosus (SLE)
NCT01705977PHASE4COMPLETEDBelimumab Assessment of Safety in SLE
NCT01753401PHASE4COMPLETEDActhar for the Treatment of Systemic Lupus Erythematosus (SLE) in Patients With a History of Persistently Active Disease
NCT02270970PHASE4UNKNOWNEvaluation of Belimumab Impact on a BLyS Activity Signature Test in the Absence of Confounding Polypharmacy
NCT02477150PHASE4COMPLETEDSafety and Immunogenicity of a Zoster Vaccine in SLE
NCT02741960PHASE4COMPLETEDThe Effect of Metformin on Reducing Lupus Flares
NCT02779153PHASE4WITHDRAWNActhar SLE (Systemic Lupus Erythematosus)
NCT02953821PHASE4COMPLETEDActhar Gel for Active Systemic Lupus Erythematosus (SLE)
NCT03042260PHASE4UNKNOWNProphylactic Trimethoprim/Sulfamethoxazole to Prevent Severe Infections in Patients With Lupus Erythematous
NCT03098823PHASE4COMPLETEDA Crossover Study to Compare RAYOS to IR Prednisone to Improve Fatigue and Morning Symptoms for SLE
NCT03122431PHASE4COMPLETEDRelevance of Monitoring Blood and Salivar Levels of Drugs Used in Rheumatic Autoimmune Diseases
NCT03543839PHASE4RECRUITINGTrial of Belimumab in Early Lupus
NCT04447053PHASE4UNKNOWNSequential Belimumab and T-cell Based Therapy in SLE
NCT04515719PHASE4COMPLETEDEfficacy and Safety of Belimumab in SLE Patients
NCT04893161PHASE4UNKNOWNA Model About the Response of Belimumab in SLE
NCT04908865PHASE4COMPLETEDOpen-label Study of Belimumab Plus Standard Therapy in Chinese Pediatric Participants With Active Systemic Lupus Erythematosus (SLE)
NCT04956484PHASE4COMPLETEDBelimumab In Early Systemic Lupus Erythematosus
NCT05559671PHASE4RECRUITINGSafety of the Herpes Zoster Subunit Vaccine in Lupus
NCT05666336PHASE4UNKNOWNMulti-omics Studies on the Efficacy of Telitacicept in Chinese SLE Patients
NCT05748925PHASE4COMPLETEDCardio Renal Effects of SGLT2 Inhibitors Among Lupus Nephritis Patients