Literature DB >> 34263318

Contribution of Schistosoma mansoni to systemic inflammation and microbial translocation among people with HIV in Zambia.

Briana D Furch1,2, Simutanyi Mwakamui1, Sandie Sianongo3, Kanekwa Zyambo1, Douglas C Heimburger2,4, John R Koethe2, Paul Kelly1,5.   

Abstract

BACKGROUND: Schistosoma mansoni is hyperendemic in many rural areas of Zambia where up to 77% of people are positive for infection via serologic evaluation. Zambia also has a high prevalence of HIV infection. Individually, S. mansoni and HIV infection impair gastrointestinal barrier integrity and induce inflammation, but the effects of coinfection are not well understood. We set out to test the hypothesis that HIV would exacerbate intestinal barrier failure in patients with S. mansoni infection.
METHODS: Adults attending medical outpatient clinics in Kaoma, Western Province, Zambia, were enrolled in a case-control study to determine the relative contributions of schistosomiasis and HIV to microbial translocation (measured as soluble CD14 [sCD14] and lipopolysaccharide binding protein [LBP]) and inflammation (measured as CRP).
RESULTS: Among 152 adults evaluated, 74 (49%) were HIV-seropositive, 45 (29%) were shedding schistosome ova (Kato-Katz), 120 (81%) were seropositive for schistosome antibodies (i.e. prior or current infection, with or without egg shedding) and 16 (11%) were HIV/schistosome coinfected (defined by Kato-Katz). HIV infection was associated with higher circulating sCD14 concentrations (p=0.003 by Kruskal-Wallis test), but schistosomiasis was not. HIV infection was associated with greater exposure to schistosomes assessed serologically (OR=2.48, 95% CI 1.05 to 5.86; p=0.03), but reduced likelihood of egg shedding (OR 0.47, 95% CI 0.21 to 1.01; p=0.03).
CONCLUSIONS: There was no evidence for a compounding or synergistic effect of coinfection on microbial translocation that appeared to be correlated with HIV infection. Further studies are needed to understand how the increase in LBP secondary to HIV infection may decrease schistosome egg excretion in coinfected individuals.
© The Author(s) 2021. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene.

Entities:  

Keywords:  HIV; Schistosomiasis; Zambia; inflammation; microbial translocation

Mesh:

Substances:

Year:  2022        PMID: 34263318      PMCID: PMC8804879          DOI: 10.1093/trstmh/trab103

Source DB:  PubMed          Journal:  Trans R Soc Trop Med Hyg        ISSN: 0035-9203            Impact factor:   2.455


  32 in total

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4.  Treatment of Schistosoma mansoni infection increases helminth-specific type 2 cytokine responses and HIV-1 loads in coinfected Ugandan adults.

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7.  Association of Macrophage Inflammation Biomarkers With Progression of Subclinical Carotid Artery Atherosclerosis in HIV-Infected Women and Men.

Authors:  David B Hanna; Juan Lin; Wendy S Post; Howard N Hodis; Xiaonan Xue; Kathryn Anastos; Mardge H Cohen; Stephen J Gange; Sabina A Haberlen; Sonya L Heath; Jason M Lazar; Chenglong Liu; Wendy J Mack; Igho Ofotokun; Frank J Palella; Phyllis C Tien; Mallory D Witt; Alan L Landay; Lawrence A Kingsley; Russell P Tracy; Robert C Kaplan
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8.  Prevention and control of schistosomiasis: a current perspective.

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9.  Schistosoma mansoni infection and socio-behavioural predictors of HIV risk: a cross-sectional study in women from Uganda.

Authors:  Sergey Yegorov; Ronald M Galiwango; Sara V Good; Juliet Mpendo; Egbert Tannich; Andrea K Boggild; Noah Kiwanuka; Bernard S Bagaya; Rupert Kaul
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Review 10.  Impact of Endemic Infections on HIV Susceptibility in Sub-Saharan Africa.

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