A novel association of efavirenz induced severe cutaneous adverse reactions with HLA‐ DRB1*03:01: A case‐control study from North‐East India

HIV‐infected patients have a higher risk of developing cutaneous reactions to drugs than the general population. Severe cutaneous adverse reactions (SCARs) are not uncommon in patients taking antiretroviral therapy (HAART]. To evaluate HLA class I and II allele frequencies in HIV patients on HAART who develop SCARs due to nevirapine (NVP] or efavirenz (EFZ] containing regime and compare this genotype composition with HAART tolerant patients and healthy organ donors. A case‐control study for 4 years was conducted with four subsets of patients hailing from north‐east India:Cohort 1‐ HIV seropositive patients who developed SCARs due to EFZ (n = 8];Cohort 2 ‐ HIV seropositive patients who developed SCARs due to NVP (n = 15]; Cohort 3 ‐HIV seropositive NVP/EFZ‐tolerant patients (n = 18]; Cohort 4 ‐ Healthy HIV seronegative organ donors (n = 169].Cohort 3 & 4 acted as control‐group. These patients were genotyped for the HLA‐A, HLA‐B, HLA‐C, HLA‐DRB1, HLA‐DQB1, and HLA‐DPB1 by a sequence‐based HLA typing method. HLA‐DRB1*03:01 allele revealed a significant association with EFZ regimen‐induced SCARs in 62.5% patients compared with only 5.56% observed in HAART‐tolerant patients and 4.14% in healthy organ. HLA‐B*3505was found to be significantly associated with NVP induced SCARs. We found significant novel association of HLA‐DRB1*03:01 with EFZ induced SCARs in North‐East Indian HIV patients. Thus, HLA‐DRB*03:01 may be useful as a genetic marker to avoid EFZ induced serious cutaneous rashes. The molecular HLA characterization of these alleles may provide a novel insight into the immunological basis of the antiretroviral drug reactions.

[1]  S. Mallal,et al.  Active suppression rather than ignorance: tolerance to abacavir‐induced HLA‐B*57:01 peptide repertoire alteration , 2018, The Journal of clinical investigation.

[2]  P. Wolkenstein,et al.  Severe cutaneous adverse reactions to drugs , 2017, The Lancet.

[3]  David Brandariz,et al.  Drug reaction with eosinophilia and systemic symptoms related to antiretroviral treatment in human immunodeficiency virus patients , 2017, Indian journal of sexually transmitted diseases and AIDS.

[4]  P. Deloukas,et al.  Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population , 2017, The Journal of antimicrobial chemotherapy.

[5]  H. Koochak,et al.  Prevalence of Adverse Drug Reactions to Highly Active Antiretroviral Therapy (HAART) among HIV Positive Patients in Imam Khomeini Hospital of Tehran, Iran. , 2017, Infectious disorders drug targets.

[6]  S. Sen,et al.  A Suspected Case of Efavirenz-Induced Stevens–Johnson Syndrome , 2015, Drug Safety - Case Reports.

[7]  F. Sarfo,et al.  Incidence and Determinants of Nevirapine and Efavirenz-Related Skin Rashes in West Africans: Nevirapine's Epitaph? , 2014, PloS one.

[8]  L. Miao,et al.  Association between the HLA-B*15:02 allele and carbamazepine-induced Stevens-Johnson syndrome/toxic epidermal necrolysis in Han individuals of northeastern China , 2013, Pharmacological reports : PR.

[9]  D. Chilton,et al.  Raltegravir-induced drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome: implications for clinical practice and patient safety , 2010, Journal of the International AIDS Society.

[10]  O. Mir,et al.  Raltegravir-induced DRESS syndrome , 2012, Scandinavian journal of infectious diseases.

[11]  Kevin S. Zhang,et al.  DRESS syndrome associated with raltegravir. , 2011, Dermatology online journal.

[12]  K. Ghosh,et al.  HLA involvement in nevirapine-induced dermatological reaction in antiretroviral-treated HIV-1 patients , 2011, Journal of pharmacology & pharmacotherapeutics.

[13]  Yusuke Nakamura,et al.  HLA-B*3505 allele is a strong predictor for nevirapine-induced skin adverse drug reactions in HIV-infected Thai patients , 2009, Pharmacogenetics and genomics.

[14]  Y. Marfatia,et al.  Adverse effects of antiretroviral treatment. , 2008, Indian journal of dermatology, venereology and leprology.

[15]  A. Hovnanian,et al.  HLA-DRB1*01 associated with cutaneous hypersensitivity induced by nevirapine and efavirenz , 2008, AIDS.

[16]  H. Yazaki,et al.  HLA-Cw8 primarily associated with hypersensitivity to nevirapine. , 2007, AIDS.

[17]  S. Jee,et al.  Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions , 2006, Pharmacogenetics and genomics.

[18]  A. Krieger,et al.  Acute respiratory manifestations of the abacavir hypersensitivity reaction. , 2006, AIDS.

[19]  C. Moore,et al.  Predisposition to nevirapine hypersensitivity associated with HLA-DRB1*0101 and abrogated by low CD4 T-cell counts , 2005, AIDS.

[20]  D. Metry,et al.  Stevens-Johnson syndrome caused by the antiretroviral drug nevirapine. , 2001, Journal of the American Academy of Dermatology.

[21]  R. Chaisson,et al.  Highly Active Antiretroviral Therapy in a Large Urban Clinic: Risk Factors for Virologic Failure and Adverse Drug Reactions , 1999, Annals of Internal Medicine.

[22]  R. Pollard,et al.  Safety profile of nevirapine, a nonnucleoside reverse transcriptase inhibitor for the treatment of human immunodeficiency virus infection. , 1998, Clinical therapeutics.