Association Between Plasma Antibody Responses and Risk for Cryptococcus-Associated Immune Reconstitution Inflammatory Syndrome

Author:

Yoon Hyun Ah1,Nakouzi Antonio2,Chang Christina C3,Kuniholm Mark H4,Carreño Leandro J5,Wang Tao6,Ndung’u Thumbi78910,Lewin Sharon R311,French Martyn A12,Pirofski Liise-anne1

Affiliation:

1. Department of Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York

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

3. Department of Infectious Diseases, Alfred Hospital and Monash University, Melbourne, Australia

4. Department of Epidemiology and Biostatistics, University at Albany, Rensselaer, New York

5. Millennium Institute on Immunology and Immunotherapy, Programa de Inmunología, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Santiago, Chile

6. Department of Epidemiology and Population Health, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York

7. HIV Pathogenesis Programme, Doris Duke Medical Research Institute, Nelson R Mandela School of Medicine, University of KwaZulu-Natal

8. Africa Health Research Institute, Durban, South Africa

9. Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge

10. Max Planck Institute for Infection Biology, Berlin, Germany

11. The Peter Doherty Institute for Infection and Immunity, University of Melbourne and Royal Melbourne Hospital

12. University of Western Australia Medical School and School of Biomedical Sciences, Perth, Australia

Abstract

AbstractBackgroundInitiation of antiretroviral therapy (ART) in human immunodeficiency virus (HIV)-infected individuals with cryptococcal meningitis places them at risk for Cryptococcus-associated immune reconstitution inflammatory syndrome (C-IRIS). The relationship between antibody immunity and C-IRIS risk has not been investigated.MethodsWe compared plasma levels of immunoglobulins, C. neoformans glucuronoxylomannan (GXM) capsule-specific and laminarin (Lam)-binding IgM and IgG, and percentages of peripheral blood total and memory B cells between 27 HIV-infected patients with CM who developed C-IRIS and 63 who did not, and evaluated associations of these parameters with risk of C-IRIS.ResultsPrior to initiation of ART, plasma IgM, Lam-binding IgM (Lam-IgM), Lam-IgG, and GXM-IgM levels were significantly lower in patients who developed C-IRIS than those who did not. Multivariate analysis revealed significant inverse associations between C-IRIS and IgM (P = .0003), Lam-IgM (P = .0005), Lam-IgG (P = .002), and GXM-IgM (P = .002) independent of age, sex, HIV viral load, CD4+ T-cell count, and cerebrospinal fluid fungal burden. There were no associations between C-IRIS and total or memory B cells.DiscussionAntibody profiles that include plasma IgM, Lam-IgM, Lam-IgG, and/or GXM-IgM may have value in furthering our understanding of C-IRIS pathogenesis and hold promise as candidate biomarkers of C-IRIS risk.

Funder

National Institutes of Health

Australian National Health and Medical Research Council

Howard Hughes Medical Institute

Wellcome Trust

South African National Research Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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