Increased HIV Incidence in Wuchereria bancrofti Microfilaria Positive Individuals in Tanzania

Author:

Mnkai Jonathan1,Ritter Manuel2ORCID,Maganga Lucas1,Maboko Leonard13,Olomi Willyhelmina1,Clowes Petra1,Minich Jessica2,Lelo Agola Eric4,Kariuki Daniel5,Debrah Alexander Yaw6ORCID,Geldmacher Christof78,Hoelscher Michael78,Saathoff Elmar78ORCID,Chachage Mkunde19ORCID,Pfarr Kenneth210ORCID,Hoerauf Achim21011ORCID,Kroidl Inge78

Affiliation:

1. National Institute of Medical Research (NIMR), Mbeya Medical Research Center (MMRC), Mbeya P.O. Box 2410, Tanzania

2. Institute for Medical Microbiology, Immunology and Parasitology (IMMIP), University Hospital Bonn (UKB), 53127 Bonn, Germany

3. Tanzania Commission for AIDS, Dodoma P.O. Box 2904, Tanzania

4. Kenya Medical Research Institute (KEMRI), KNH, Nairobi, Kenya

5. College of Health Sciences, Jomo Kenyatta University of Agriculture and Technology (JKUAT), Juja, Kenya

6. Kumasi Centre for Collaborative Research (KCCR), Kwame Nkrumah University of Science and Technology, UPO, PMB, Kumasi, Ghana

7. Division of Infectious Diseases and Tropical Medicine, University Hospital of the University of Munich (LMU), 80802 Munich, Germany

8. German Centre for Infection Research (DZIF), Partner Site Munich, 80802 Munich, Germany

9. Mbeya College of Health and Allied Sciences (UDSM-MCHAS), University of Dar es Salaam, Mbeya 608, Tanzania

10. German Centre for Infection Research (DZIF), Partner Site Bonn-Cologne, 53127 Bonn, Germany

11. German-West African Centre for Global Health and Pandemic Prevention (G-WAC), Partner Site Bonn, 53127 Bonn, Germany

Abstract

Background: Infections with Wuchereria bancrofti are associated with reduced immunity against concomitant infections. Indeed, our previous study described a 2.3-fold increased HIV incidence among individuals with W. bancrofti infection, as measured by the circulating filarial antigen of the adult worm. This new study aimed to retrospectively determine microfilariae status of the participants to assess if the previously described increased HIV susceptibility was associated with the presence of MF in the same cohort. Methods: CFA positive but HIV negative biobanked human blood samples (n = 350) were analyzed for W. bancrofti MF chitinase using real time PCR. Results: The PCR provided a positive signal in 12/350 (3.4%) samples. During four years of follow-up (1109 person years (PY)), 22 study participants acquired an HIV infection. In 39 PY of W. bancrofti MF chitinase positive individuals, three new HIV infections occurred (7.8 cases per 100 PY), in contrast to 19 seroconversions in 1070 PY of W. bancrofti MF chitinase negative individuals (1.8 cases per 100 PY, p = 0.014). Conclusions: In the subgroup of MF-producing Wb-infected individuals, the HIV incidence exceeded the previously described moderate increased risk for HIV seen in all Wb-infected individuals (regardless of MF status) compared with uninfected persons from the same area.

Funder

Germany Research Foundation

European Commission

Germany Center for Infection Research

German Federal Ministry of Education and Research (BMBF) and the Ministry of Culture and Science of the State of North Rhine-Westphalia

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

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