PMID- 35519172 OWN - NLM STAT- MEDLINE DCOM- 20220509 LR - 20220716 IS - 1937-8688 (Electronic) VI - 41 DP - 2022 TI - Association between human leukocyte antigen class II (HLA-DRB and -DQB) alleles and outcome of exposure to Mycobacterium tuberculosis: a cross-sectional study in Nairobi, Kenya. PG - 149 LID - 10.11604/pamj.2022.41.149.30056 [doi] LID - 149 AB - INTRODUCTION: human leukocyte antigen (HLA) class II alleles play an important role in the early immune response to tuberculosis (TB) by presenting antigenic peptides to CD4+ T cells, hence polymorphisms in those genes can influence the efficiency of the immune response to infection and progression to active disease. METHODS: an analytical cross-sectional study of adult pulmonary tuberculosis (PTB) patients at Mbagathi County Hospital, Nairobi and their HHCs. Sociodemographic data were captured on questionnaires and clinical data extracted from patient files. Intravenous blood samples were drawn for interferon-gamma release assay (IGRA) to determine latent tuberculosis infection (LTBI) among HHCs, and for extraction of DNA used in typing of HLA-DQB1 and HLA-DRB1 alleles by PCR sequence specific primer amplification. Chi-square and Fisher's exact test were used to compare the HLA type II allele frequencies of LTBI negative HHCs, LTBI positive HHCs and active TB patients. Logistic regression was used to adjust for HIV status. RESULTS: the HLA-DQB1 and HLA-DRB1 alleles were analyzed in 17 PTB and 37 HHCs. Nineteen (19) HHCs were LTBI positive, while 18 were LTBI negative. The frequency of DRB3*1 was 0.17-fold lower [95% CI=0.03-0.83] among PTB patients compared to HHCs before adjustment for HIV status (p=0.048). The frequency of the DRB5*2 allele was significantly higher (p=0.013) among PTB patients (23.5%) compared to HHCS (0.00%). After adjusting for HIV status, the frequency of DRB1*14 was 12-fold higher [95% CI=1.11-138.2] among PTB patients compared to HHCs (p=0.040). CONCLUSION: the higher frequencies of HLA-DRB5*2 and HLA-DRB1*14 alleles in PTB patients suggest a likely association with progression to active PTB. The higher frequency of HLA-DRB3*1 allele among LTBI negative HHCs shows its likely protective role against M. tuberculosis infection in this population. CI - Copyright: Susan Odera et al. FAU - Odera, Susan AU - Odera S AD - Department of Medical Microbiology and Immunology, University of Nairobi, Nairobi, Kenya. FAU - Mureithi, Marianne AU - Mureithi M AD - Department of Medical Microbiology and Immunology, University of Nairobi, Nairobi, Kenya. AD - Kenya Aids Vaccine Initiative (KAVI) Institute of Clinical Research, University of Nairobi, Nairobi, Kenya. FAU - Aballa, Andrew AU - Aballa A AD - Department of Medical Laboratory Sciences, School of Medicine, Kenyatta University, Nairobi, Kenya. FAU - Onyango, Noel AU - Onyango N AD - Department of Clinical Medicine and Therapeutics, School of Medicine, University of Nairobi, Nairobi, Kenya. FAU - Kazungu, Samwel AU - Kazungu S AD - Kenya Aids Vaccine Initiative (KAVI) Institute of Clinical Research, University of Nairobi, Nairobi, Kenya. FAU - Ogolla, Simon AU - Ogolla S AD - Kenya Aids Vaccine Initiative (KAVI) Institute of Clinical Research, University of Nairobi, Nairobi, Kenya. FAU - Kaiyare, George AU - Kaiyare G AD - Biozeq Kenya Molecular Laboratory, Nairobi, Kenya. FAU - Anzala, Omu AU - Anzala O AD - Department of Medical Microbiology and Immunology, University of Nairobi, Nairobi, Kenya. AD - Kenya Aids Vaccine Initiative (KAVI) Institute of Clinical Research, University of Nairobi, Nairobi, Kenya. FAU - Oyugi, Julius AU - Oyugi J AD - Department of Medical Microbiology and Immunology, University of Nairobi, Nairobi, Kenya. AD - Institute of Tropical and Infectious Diseases, University of Nairobi, Nairobi, Kenya. LA - eng PT - Journal Article DEP - 20220221 PL - Uganda TA - Pan Afr Med J JT - The Pan African medical journal JID - 101517926 RN - 0 (HLA-DRB1 Chains) SB - IM MH - Adult MH - Alleles MH - Cross-Sectional Studies MH - Gene Frequency MH - *HIV Infections MH - HLA-DRB1 Chains/genetics MH - Humans MH - Kenya MH - *Latent Tuberculosis/epidemiology/genetics MH - *Mycobacterium tuberculosis/genetics MH - *Tuberculosis, Lymph Node MH - *Tuberculosis, Pulmonary/epidemiology/genetics PMC - PMC9046861 OTO - NOTNLM OT - Human leucocyte antigen OT - Kenya OT - household contacts OT - latent tuberculosis OT - pulmonary tuberculosis COIS- The authors declare no competing interest. EDAT- 2022/05/07 06:00 MHDA- 2022/05/10 06:00 PMCR- 2022/02/21 CRDT- 2022/05/06 06:03 PHST- 2021/05/28 00:00 [received] PHST- 2022/02/02 00:00 [accepted] PHST- 2022/05/06 06:03 [entrez] PHST- 2022/05/07 06:00 [pubmed] PHST- 2022/05/10 06:00 [medline] PHST- 2022/02/21 00:00 [pmc-release] AID - PAMJ-41-149 [pii] AID - 10.11604/pamj.2022.41.149.30056 [doi] PST - epublish SO - Pan Afr Med J. 2022 Feb 21;41:149. doi: 10.11604/pamj.2022.41.149.30056. eCollection 2022.