Immune reconstitution inflammatory syndrome

disease
On this page

Also known as immune reconstitution inflammatory syndrome associated with Kaposi sarcomaimmune reconstitution syndromeimmune restoration diseaseIRDIRISIRS

Summary

Immune reconstitution inflammatory syndrome (MONDO:0100185) is a disease and 13 clinical trials. Top therapeutic interventions include prednisolone, methylprednisolone, and naproxen. A subtype of immune system disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 13

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameimmune reconstitution inflammatory syndrome
Mondo IDMONDO:0100185
MeSHD054019
ICD-10-CMD89.3
ICD-11180703474
NCITC125712
UMLSC1619738
MedGen295297
Is cancer (heuristic)no

Also known as: immune reconstitution inflammatory syndrome associated with Kaposi sarcoma · immune reconstitution syndrome · immune restoration disease · IRD · IRIS · IRS

Disease family

This is a subtype of immune system disorder. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › immune system disorderimmune reconstitution inflammatory syndrome

Related subtypes (46): hypersensitivity reaction disease, immune system cancer, immune system organ benign neoplasm, bone marrow disorder, thymus gland disorder, inborn error of immunity, leukocyte disorder, psoriasis, spondyloarthropathy, aggressive insulitis, benign insulitis, inflammatory bowel disease, autoimmune disease, TNF receptor 1-associated periodic fever syndrome, epidermodysplasia verruciformis, Vici syndrome, proteosome-associated autoinflammatory syndrome, hyperimmunoglobulinemia D with periodic fever, transcobalamin II deficiency, pyogenic arthritis-pyoderma gangrenosum-acne syndrome, granulomatosis with polyangiitis, autosomal recessive osteopetrosis 7, graft versus host disease, congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome, Roifman syndrome, cryopyrin-associated periodic syndrome, anti-HLA hyperimmunization, acquired immunodeficiency, erythroderma desquamativum, autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis, familial Mediterranean fever, 22q11.2 deletion syndrome, T-cell large granular lymphocyte leukemia, twin to twin transfusion syndrome, immunodeficiency disease, immunoproliferative disorder, cytokine receptor deficiency, immunodeficiency-related disorder, phagocytic cell dysfunction, thrombocytopenic purpura, lymphoid system disorder, growth hormone insensitivity with immune dysregulation 1, autosomal recessive, cytokine release syndrome, early-onset autoimmunity-autoinflammation-immunodeficiency syndrome, CADINS disease, autoinflammation, panniculitis, and dermatosis syndrome

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 13.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified8
PHASE32
PHASE41
PHASE2/PHASE31
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01211665PHASE4TERMINATEDCorticosteroids for Immune Reconstitution Inflammatory Syndrome (IRIS)
NCT01442428PHASE2/PHASE3WITHDRAWNParadoxical Tuberculosis Immune Reconstitution Inflammatory Syndrome (TB-IRIS) Treatment Trial
NCT01924286PHASE3COMPLETEDPreventing TB-IRIS in High-risk Patients: a Randomized Placebo-controlled Trial of Prednisone
NCT03092817PHASE3COMPLETEDAdjunctive Corticosteroids for Tuberculous Meningitis in HIV-infected Adults (The ACT HIV Trial)
NCT03296553PHASE2COMPLETEDImpact of Valganciclovir on Severe IRIS-Kaposi Sarcoma Mortality: an Open-label, Parallel, Randomized Controlled-trial.
NCT02147405Not specifiedRECRUITINGPET Imaging and Lymph Node Assessment of IRIS in People With AIDS
NCT07565623Not specifiedNOT_YET_RECRUITINGPrevention of AIDS With Opportunistic Infection Paradoxical IRIS
NCT00286767Not specifiedCOMPLETEDImmune Reconstitution Syndrome in HIV-Infected Patients Taking Antiretroviral Therapy
NCT00988780Not specifiedUNKNOWNMaraviroc (CCR5) Antagonism to Decrease the Incidence of the Immune Reconstitution Inflammatory Syndrome in HIV-Infected Patients
NCT01240486Not specifiedCOMPLETEDIMPAACT P1073: Study of IRIS for Infants and Children Initiating HAART at Int’l Sites
NCT01557803Not specifiedCOMPLETEDPrediction and Pathogenesis of the Immune Reconstitution Inflammatory Syndrome
NCT02063880Not specifiedCOMPLETEDPediatric Urgent Start of Highly Active Antiretroviral Treatment (HAART)
NCT05484050Not specifiedUNKNOWNVEGF in Iris Tissue in Primary Congenital Glaucoma

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
PREDNISOLONE42
METHYLPREDNISOLONE41
NAPROXEN41
VALGANCICLOVIR41
CHEMBL161825401