Prevalence of HLA-B*57:01 allele in HIV-positive and HIV-negative population of eastern India: An epidemiological study

被引:2
作者
Gautam, Abhilasha [1 ]
Chakravarty, Jaya [1 ]
Chourasia, Ankita [1 ]
Sharma, Saurabh [1 ]
Sarkar, Tanmoy [2 ]
Das, Parimal [2 ]
机构
[1] Banaras Hindu Univ, Inst Med Sci, Dept Med, Varanasi 221005, Uttar Pradesh, India
[2] Banaras Hindu Univ, Fac Sci, Ctr Genet Disorders, Varanasi 221005, Uttar Pradesh, India
来源
CLINICAL EPIDEMIOLOGY AND GLOBAL HEALTH | 2022年 / 18卷
关键词
Abacavir; HIV; HLA-B*57:01 allele; Hypersensitivity reaction; India; HLA-B REGION; ABACAVIR HYPERSENSITIVITY; MOLECULAR DIVERSITY; GENETIC-VARIATIONS; ASSOCIATION; CHILDREN; CASTE; PCR;
D O I
10.1016/j.cegh.2022.101181
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Introduction: The nucleoside analogue reverse-transcriptase inhibitor Abacavir has potent antiviral activity against HIV; however, 5-8% patients develop hypersensitivity reactions within six weeks of treatment. The presence of the HLA-B*57:01 allele is strongly associated with the risk of Abacavir-associated hypersensitivity reaction (ABC-HSR). Prevalence of HLA-B*57:01 allele varies in different populations. This observational study was performed to determine the prevalence of HLA-B*57:01 allele in the population of Eastern India which included both HIV-positive and HIV-negative subjects. Methods: We screened 406 subjects attending the ART (antiretroviral treatment) centre and linked ICTC (Integrated counselling and testing centre), however 6 samples did not have adequate DNA. HLA-B*57:01 typing was done using direct sequence specific primer PCR (SSP-PCR). All PCR positive samples were sequenced using Sanger's method. Results: The prevalence of HLA-B*57:01 genotype in our cohort was 12.25% (49/400). Prevalence among men was 13.3% (33/248) and female was 10.5% (16/152). The prevalence was similar in HIV-positive subjects (13.5%) and in HIV-negative subjects (11%). Conclusions: Prevalence of HLA-B*57:01 in our eastern Indian population was high. Therefore, screening for HLAB*57:01 before ABC administration would be useful to prevent ABC-HSR.
引用
收藏
页数:5
相关论文
共 25 条
[1]  
[Anonymous], 2016, NACO ANN REP 2016 20, P1
[2]  
Balakrishnan K, 1996, HUM BIOL, V68, P523
[3]   Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 [J].
Cascella, R. ;
Strafella, C. ;
Ragazzo, M. ;
Zampatti, S. ;
Borgiani, P. ;
Gambardella, S. ;
Pirazzoli, A. ;
Novelli, G. ;
Giardina, E. .
PHARMACOGENOMICS JOURNAL, 2015, 15 (02) :196-200
[4]   Clinical Abacavir Hypersensitivity Reaction among Children in India [J].
Chakravarty, Jaya ;
Sharma, Saurabh ;
Johri, Anuradha ;
Chourasia, Ankita ;
Sundar, Shyam .
INDIAN JOURNAL OF PEDIATRICS, 2016, 83 (08) :855-858
[5]   Human leukocyte antigen B distribution in HIV discordant cohort from India [J].
Chaudhari, Deepali V. ;
Chavan, Vijay R. ;
Ahir, Swati P. ;
Kerkar, Shilpa C. ;
Mehta, Preeti R. ;
Mania-Pramanik, Jayanti .
IMMUNOLOGY LETTERS, 2013, 156 (1-2) :1-6
[6]   Genetic variation among the Golla pastoral caste subdivisions of Andhra Pradesh, India, according to the HLA system [J].
Crawford, MH ;
Reddy, BM ;
Martinez-Laso, J ;
Mack, SJ ;
Erlich, HA .
HUMAN IMMUNOLOGY, 2001, 62 (09) :1031-1041
[7]  
Dedhia L., 2015, Ind. J. Transplan., V9, P138, DOI [10.1016/j.ijt.2015.10.016, DOI 10.1016/J.IJT.2015.10.016]
[8]   Allele frequency net: a database and online repository for immune gene frequencies in worldwide populations [J].
Gonzalez-Galarza, Faviel F. ;
Christmas, Stephen ;
Middleton, Derek ;
Jones, Andrew R. .
NUCLEIC ACIDS RESEARCH, 2011, 39 :D913-D919
[9]   Genetic variations in HLA-B region and hypersensitivity reactions to abacavir [J].
Hetherington, S ;
Hughes, AR ;
Mosteller, M ;
Shortino, D ;
Baker, KL ;
Spreen, W ;
Lai, E ;
Davies, K ;
Handley, A ;
Dow, DJ ;
Fling, ME ;
Stocum, M ;
Bowman, C ;
Thurmond, LM ;
Roses, AD .
LANCET, 2002, 359 (9312) :1121-1122
[10]   Association of genetic variations in HLA-B region with hypersensitivity to abacavir in some, but not all, populations [J].
Hughes, AR ;
Mosteller, M ;
Bansal, AT ;
Davies, K ;
Haneline, SA ;
Lai, EH ;
Nangle, K ;
Scott, T ;
Spreen, WR ;
Warren, LL ;
Roses, AD .
PHARMACOGENOMICS, 2004, 5 (02) :203-211