Shared and unique antibody and B cell profiles in HIV-positive and HIV-negative individuals with cryptococcal meningoencephalitis

Author:

Yoon Hyunah1ORCID,Nakouzi Antonio S2,Duong Van Anh3,Hung Le Quoc4,Binh Tran Quang4,Tung Nguyen Le Nhu5,Day Jeremy N36ORCID,Pirofski Liise-anne12

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine, Montefiore Medical Center , Bronx, New York 10461 , USA

2. Department of Microbiology and Immunology, Albert Einstein College of Medicine, Montefiore Medical Center , Bronx, New York 10461 , USA

3. Oxford University Clinical Research Unit , 764 Vo Van Kiet, Ho Chi Minh City Q5 , Vietnam

4. Department of Tropical Diseases, Cho Ray Hospital , Ho Chi Minh City , Vietnam

5. Hospital for Tropical Diseases , 764 Vo Van Kiet, Ho Chi Minh City Q5 , Vietnam

6. Department of Microbiology and Infection, Royal Devon and Exeter Hospital , Exeter EX2 5DW , UK

Abstract

Abstract Host non-T cell markers to aid in the diagnosis of cryptococcal meningoencephalitis (CM) have not been identified. In this case-control study, we characterized antibody and B cell profiles in HIV-negative and HIV-positive Vietnamese individuals of the Kinh ethnicity recently diagnosed with CM and controls. The study included 60 HIV-negative with no known immunocompromising condition and 60 HIV-positive individuals, with 30 CM cases and 30 controls in each group. Participants were matched by age, sex, HIV serostatus, and CD4 count in the HIV-positive group. Plasma immunoglobulin (Ig) levels, including IgG1, IgG2, IgM, and IgA, Cryptococcus spp. glucuronoxylomannan (GXM)- and laminarin (branched ${\rm{\beta }}$-[1-3]-glucan)-binding IgG, IgM, IgA levels, and peripheral blood B cell subsets were measured. Logistic regression, principal component, and mediation analyses were conducted to assess associations between antibody, B cell levels, and CM. The results showed that GXM-IgG levels were higher and IgG1 and IgG2 were lower in CM cases than controls, regardless of HIV status. In HIV-negative individuals, IgG2 mediated an inverse association between CD19+CD27+CD43+CD5− (B-1b-like) cells and CM. In HIV-positive individuals, lower levels of IgA, laminarin-IgA, and CD19+CD27+IgM+IgD− (IgM+ memory B) cells were each associated with CM. The shared and distinct antibody and B cell profiles identified in HIV-negative and HIV-positive CM cases may inform the identification of non-T-cell markers of CM risk or unsuspected disease, particularly in HIV-negative individuals.

Funder

National Institutes of Health

City University of New York

NCATS

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,General Medicine

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