Mycobacterial antibody levels and immune restoration disease in HIV patients treated in South East Asia

Author:

Sumatoh Hermi R1,Oliver Benjamin G1,Kumar Manoj2,Elliott Julian H3,Vonthanak Saphonn4,Vun Mean Chhi5,Singh Sarman2,Agarwal Upasna6,Kumar Amitabh6,Tan Hong Yien7,Kamarulzaman Adeeba7,Yunihastuti Evy8,Saraswati Heni9,Price Patricia10

Affiliation:

1. School of Pathology & Laboratory Medicine, University of Western Australia, Perth, Australia

2. Department of Laboratory Medicine, All India Institute of Medical Sciences, New Delhi, India

3. Alfred Hospital, Melbourne, Australia and Burnet Institute for Medical Research & Public Health, Melbourne, Victoria, Australia and National Centre in HIV Epidemiology & Clinical Research, University of New South Wales, Sydney, Australia

4. National Centre for HIV/AIDS, Dermatology & Sexually Transmitted Diseases, Phnom Penh, Cambodia and National Institute of Public Health, Phnom Penh, Cambodia

5. National Institute of Public Health, Phnom Penh, Cambodia

6. LRS Institute of Tuberculosis and Respiratory Diseases, New Delhi, India

7. University of Malaya Medical Centre, Kuala Lumpur, Malaysia

8. Department of Internal Medicine, University of Indonesia, Jakarta, Indonesia

9. Institute of Human Virology & Cancer Biology, University of Indonesia, Jakarta, Indonesia.

10. School of Pathology and Laboratory Medicine University of Western Australia, M576 Level 2 Medical Research Foundation Building, Rear 50 Murray Street, Perth, WA 6000, Australia and Clinical Immunology & Immunogenetics, Royal Perth Hospital, Australia.

Abstract

Aim: Immune restoration disease (IRD) associated with Mycobacterium tuberculosis parallels the reconstitution of a pathogen-specific Th1 response. However, it is not clear whether humoral responses to M. tuberculosis antigens also rise, or whether antibody levels predict IRD. Here, humoral immunity to M. tuberculosis antigens was investigated in four Asian cohorts. Methods: Plasma samples were obtained from longitudinal prospective studies of HIV patients beginning antiretroviral therapy (ART) in New Delhi (India), Kuala Lumpur (Malaysia), Jakarta (Indonesia) and Phnom Penh (Cambodia). IgG antibodies to purified protein derivative, lipoarabinomannan and 38-kDa antigens of M. tuberculosis were quantitated using in-house ELISAs. IRD was defined as exacerbated symptoms of tuberculosis in patients on anti-tuberculosis therapy or a novel presentation of tuberculosis on ART. Results: Pre-ART IgG levels to purified protein derivative, lipoarabinomannan and 38-kDa antigen were similar in the IRD and control groups from each site. Compared with non-IRD controls, a higher proportion of IRD patients had elevated IgG levels to lipoarabinomannan (defined as a greater than twofold increase) over 12 weeks of ART. However, this trend was not significant for the other antigens and longitudinal analyses did not reveal clear rises in antibody levels at the time of IRD. Conclusion: Levels of antibody to mycobacterial antigens do not predict IRD, but levels of antibody reactive with lipoarabinomannan rise during an IRD in some patients.

Publisher

Future Medicine Ltd

Subject

Biochemistry (medical),Clinical Biochemistry,Drug Discovery

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