Immunological Responses to Helminths and HIV-1 Co-Infections

Authors

  • Elton Chavura Swansea University, Faculty of Medicine, Health and Life Science, Wales, United Kingdom
  • Wales Singini Mzuzu University, Faculty of Environmental Science, Mzuzu, Malawi
  • Russel Chidya Mzuzu University, Faculty of Environmental Science, Mzuzu, Malawi
  • Balwani Chingatichifwe Mbakaya University of Livingstonia, Department of Public Health, Malawi

Keywords:

Helminths, Water, Sanitation and Hygiene, HIV/AIDS, CD4 count, HIV-1 RNA, Viral load, HIV disease progression

Abstract

Helminth infections result from either ingestion or contact with contaminated fecal matter. To date, there is insufficient evidence as to whether helminths have influence on HIV-1 specific immune responses as literature results are indeterminate. We evaluated the effect of helminth infections on HIV disease progression through the monitoring of 2 outcomes: (1) plasma HIV-1 RNA Viral load (V/L) and (2) Cluster of Differentiation (CD4+) T-lymphocyte count amongst helminth-HIV-1 co-infected persons. We hypothesized that (1) concurrent helminth infections may damage immune control, resulting in escalating VL and reduced CD4+ T-lymphocyte count (2) and that, subject to successful treatment, a decrease in plasma VL could slow down disease progression. We reviewed 2032 citations, evaluated 432 abstracts, and read 10 articles (See PRISMA diagram). The methodologies were appraised using a Mixed Method Appraisal Tool (MMAT). At enrolment, plasma VL were significantly higher in individuals with helminths (5.01 log10 vs. 3.41 log10, p < 0.001). The magnitude of effect ranged from 5.28 log10 copies/mL at baseline and 4.67 log10 copies/mL, (p < 0.05) after treatment and a trend for 0.61 log10 lower VL. All but one RCT reported decline in plasma VL and significant interactions were seen in the successfully treated groups (p < 0.001). CD4+ T-lymphocyte count values were not significantly different in the co-infection groups relative to those with HIV-infection alone. This evidence supports that WaSH and HIV/AIDS co-programming could promote health of PLWHA. We suggest large scale trials for future studies. This systematic review registration number is CRD42022364296.

 

References

Adeleke, O.A., Yogeswaran, P. and Wright, G., 2015. Intestinal

helminth infections amongst HIV-infected adults in Mthatha

General Hospital, South Africa. African Journal of Primary

Health Care and Family Medicine, 7(1), pp.1-7.

Alsan, M.M., Westerhaus, M., Herce, M., Nakashima, K. and Farmer,

P.E., 2011. Poverty, global health, and infectious disease: lessons

from Haiti and Rwanda. Infectious Disease Clinics, 25(3), pp.611-

Azoh Barry, J., 2014. Social sciences research on infectious diseases

of poverty: too little and too late?. PLoS neglected tropical

diseases, 8(6), p.e2803.

Bangert, M., Molyneux, D.H., Lindsay, S.W., Fitzpatrick, C. and

Engels, D., 2017. The cross-cutting contribution of the end of

neglected tropical diseases to the sustainable development

goals. Infectious diseases of poverty, 6(1), pp.1-20.

Bhutta, Z.A., Sommerfeld, J., Lassi, Z.S., Salam, R.A. and Das, J.K.,

Global burden, distribution, and interventions for infectious

diseases of poverty. Infectious diseases of poverty, 3(1), pp.1-7.

Blackwell, A.D., 2016. Helminth infection during pregnancy: insights

from evolutionary ecology. International journal of women's

health, 8, p.651.

Brown, M., Kizza, M., Watera, C., Quigley, M.A., Rowland, S.,

Hughes, P., Whitworth, J.A. and Elliott, A.M., 2004. Helminth

infection is not associated with faster progression of HIV disease in

coinfected adults in Uganda. The Journal of infectious

diseases, 190(10), pp.1869-1879.

Campbell, S.J., Biritwum, N.K., Woods, G., Velleman, Y., Fleming,

F. and Stothard, J.R., 2018. Tailoring water, sanitation, and hygiene

(WASH) targets for soil-transmitted helminthiasis and

schistosomiasis control. Trends in parasitology, 34(1), pp.53-63.

Deol, A.K., Fleming, F.M., Calvo-Urbano, B., Walker, M., Bucumi,

V., Gnandou, I., Tukahebwa, E.M., Jemu, S., Mwingira, U.J.,

Alkohlani, A. and Traoré, M., 2019. Schistosomiasis—assessing

progress toward the 2020 and 2025 global goals. New England

Journal of Medicine, 381(26), pp.2519-2528.

Downs, J.A., Dupnik, K.M., van Dam, G.J., Urassa, M., Lutonja, P.,

Kornelis, D., de Dood, C.J., Hoekstra, P., Kanjala, C., Isingo, R. and

Peck, R.N., 2017. Effects of schistosomiasis on susceptibility to HIV-

infection and HIV-1 viral load at HIV-1 seroconversion: A nested

case-control study. PLoS neglected tropical diseases, 11(9),

p.e0005968.

Elliott, A.M., Ndibazza, J., Mpairwe, H., Muhangi, L., Webb, E.L.,

Kizito, D., Mawa, P., Tweyongyere, R. and Muwanga, M., 2011.

Treatment with anthelminthics during pregnancy: what gains and

what risks for the mother and child?. Parasitology, 138(12), pp.1499-

Engels, D. and Zhou, X.N., 2020. Neglected tropical diseases: an

effective global response to local poverty-related disease

priorities. Infectious diseases of poverty, 9(1), pp.1-9.

Hernández-Bello, R., Nava-Castro, K., Muñiz-Hernández, S., NavaLuna,

P., Trejo-Sánchez, I., Tiempos-Guzmán, N., MendozaRodríguez,

Y. and Morales-Montor, J., 2012. Beyond the

reproductive effect of sex steroids: their role during immunity to

helminth parasite infections. Mini reviews in medicinal

chemistry, 12(11), pp.1071- 1080.

Kallestrup, P., Zinyama, R., Gomo, E., Butterworth, A.E., van Dam,

G.J., Erikstrup, C. and Ullum, H., 2005. Schistosomiasis and HIV-1

infection in rural Zimbabwe: implications of coinfection for

excretion of eggs. The Journal of infectious diseases, 191(8),

pp.1311-1320.

Li, P., Xing, H., Zhao, Z., Yang, Z., Cao, Y., Li, W., Yan, G.,

Sattabongkot, J., Cui, L. and Fan, Q., 2015. Genetic diversity of

Plasmodium falciparum histidine-rich protein 2 in the China–

Myanmar border area. Acta tropica, 152, pp.26-31.

Mermin, J., Ekwaru, J.P., Were, W., Degerman, R., Bunnell, R.,

Kaharuza, F., Downing, R., Coutinho, A., Solberg, P., Alexander,

L.N. and Tappero, J., 2011. Utility of routine viral load, CD4

cell count, and clinical monitoring among adults with HIV

receiving antiretroviral therapy in Uganda: randomised

trial. Bmj, 343.

Modjarrad, K. and Vermund, S.H., 2010. Effect of treating coinfections

on HIV-1 viral load: a systematic review. The Lancet

infectious diseases, 10(7), pp.455-463.

Mulu, A., Maier, M. and Liebert, U.G., 2013. Deworming of

intestinal helminths reduces HIV-1 subtype C viremia in chronically

co-infected individuals. International Journal of Infectious

Diseases, 17(10), pp.e897-e901.

Mpairwe, H., Tweyongyere, R. and Elliott, A., 2014. Pregnancy and

helminth infections. Parasite immunology, 36(8), pp.328-337.

Rabiu, O.R., Dada-Adegbola, H., Falade, C.O., Arinola, O.G.,

Odaibo, A.B. and Ademowo, O.G., 2021. Malaria, Helminth

Infections and Clinical Status Among HIV-Infected Pregnant

Women. International Journal of Maternal and Child Health and

AIDS, 10(1), p.81.

Richmond, B.W., Mansouri, S., Serezani, A., Novitskiy, S.,

Blackburn, J.B., Du, R.H., Fuseini, H., Gutor, S., Han, W., Schaff, J.

and Vasiukov, G., 2021. Monocyte-derived dendritic cells link

localized secretory IgA deficiency to adaptive immune activation in

COPD. Mucosal immunology, 14(2), pp.431-442.

Sartorius, B., VanderHeide, J.D., Yang, M., Goosmann, E.A., Hon,

J., Haeuser, E., Cork, M.A., Perkins, S., Jahagirdar, D., Schaeffer,

L.E. and Serfes, A.L., 2021. Subnational mapping of HIV incidence

and mortality among individuals aged 15–49 years in sub-Saharan

Africa, 2000–18: a modelling study. The Lancet HIV, 8(6), pp.e363-

e375.

Stillwaggon, E. (2005). AIDS and the Ecology of Poverty. Oxford

University Press.

Vanhamme, L., Souopgui, J., Ghogomu, S. and Ngale Njume, F.,

The Functional Parasitic Worm Secretome: Mapping the Place

of Onchocerca volvulus Excretory

Secretory Products. Pathogens, 9(11), p.975.

Walson, J.L., Stewart, B.T., Sangaré, L., Mbogo, L.W., Otieno, P.A.,

Piper, B.K., Richardson, B.A. and John-Stewart, G., 2010.

Prevalence and correlates of helminth co-infection in Kenyan HIV-1

infected adults. PLoS neglected tropical diseases, 4(3), p.e644.

Walson, J.L., Otieno, P.A., Mbuchi, M., Richardson, B.A., LohmanPayne,

B., Macharia, S.W., Overbaugh, J., Berkley, J., Sanders, E.J.,

Chung, M. and John-Stewart, G.C., 2008. Albendazole treatment of

HIV-1 and helminth co-infection: a randomized, double blind,

placebo-controlled trial. AIDS (London, England), 22(13), p.1601.

Webb, E.L., Ekii, A.O. and Pala, P., 2012. Epidemiology and

immunology of helminth–HIV interactions. Current Opinion in HIV

and AIDS, 7(3), pp.245-253.

Wolday, D., Mayaan, S., Mariam, Z.G., Berhe, N., Seboxa, T.,

Britton, S., Galai, N., Landay, A. and Bentwich, Z., 2002. Treatment

of intestinal worms is associated with decreased HIV plasma viral

load. JAIDS-HAGERSTOWN MD-, 31(1), pp.56-62.

Woodburn, P.W., Muhangi, L., Hillier, S., Ndibazza, J., Namujju,

P.B., Kizza, M., Ameke, C., Omoding, N.E., Booth, M. and Elliott,

A.M., 2009. Risk factors for helminth, malaria, and HIV infection in

pregnancy in Entebbe, Uganda. PLoS neglected tropical

diseases, 3(6), p.e473.

World Health Organization, 2013. Global update on HIV treatment

: results, impact and opportunities.

World Health Organization, 2012. Research priorities for helminth

infections: technical report of the TDR disease reference group on

helminth infections. World Health Organization.

World Health Organization, 2011. Helminth control in school-age

children: a guide for managers of control programmes. World Health

Organization.

Downloads

Published

2023-01-30

How to Cite

Chavura, E., Singini, W., Chidya, R., & Mbakaya, B. C. (2023). Immunological Responses to Helminths and HIV-1 Co-Infections. ESI Preprints, 13, 525. Retrieved from https://esipreprints.org/index.php/esipreprints/article/view/278

Issue

Section

Preprints