CD4+ T Cell Responses to Toxoplasma gondii Are a Double-Edged Sword

Author:

El Bissati Kamal1ORCID,Krishack Paulette A.2,Zhou Ying3,Weber Christopher R.2,Lykins Joseph34,Jankovic Dragana5ORCID,Edelblum Karen L.67,Fraczek Laura3,Grover Harshita8,Chentoufi Aziz A.9ORCID,Singh Gurminder2,Reardon Catherine2ORCID,Dubey J. P.10ORCID,Reed Steve11,Alexander Jeff12,Sidney John13,Sette Alessandro13ORCID,Shastri Nilabh8,McLeod Rima3

Affiliation:

1. Institute of Molecular Engineering, University of Chicago Medical Center, Chicago, IL 60637, USA

2. Department of Pathology, University of Chicago, Chicago, IL 60637, USA

3. Department of Ophthalmology and Visual Sciences, University of Chicago, Chicago, IL 60637, USA

4. Department of Emergency Medicine, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02215, USA

5. Immunoparasitology Unit, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA

6. Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA

7. Center for Immunity and Inflammation, Laboratory Medicine, Department of Pathology, Rutgers New Jersey Medical School, Newark, NJ 07103, USA

8. Division of Immunology and Pathogenesis, Department of Molecular and Cellular Biology, University of California, Berkeley, CA 94720, USA

9. Department of Medical Microbiology, Faculty of Health Sciences, University of Pretoria, Pretoria 0028, South Africa

10. Animal Parasitic Diseases Laboratory, Beltsville Agricultural Research Center, Agricultural Research Service, U.S. Department of Agriculture, Beltsville, MD 20705, USA

11. Infectious Diseases Research Institute, 1616 Eastlake Ave E #400, Seattle, WA 98102, USA

12. PaxVax, 3985-A Sorrento Valley Blvd, San Diego, CA 92121, USA

13. La Jolla Institute of Allergy and Immunology, 9420 Athena Cir, La Jolla, CA 92037, USA

Abstract

CD4+ T cells have been found to play critical roles in the control of both acute and chronic Toxoplasma infection. Previous studies identified a protective role for the Toxoplasma CD4+ T cell-eliciting peptide AS15 (AVEIHRPVPGTAPPS) in C57BL/6J mice. Herein, we found that immunizing mice with AS15 combined with GLA-SE, a TLR-4 agonist in emulsion adjuvant, can be either helpful in protecting male and female mice at early stages against Type I and Type II Toxoplasma parasites or harmful (lethal with intestinal, hepatic, and spleen pathology associated with a storm of IL6). Introducing the universal CD4+ T cell epitope PADRE abrogates the harmful phenotype of AS15. Our findings demonstrate quantitative and qualitative features of an effective Toxoplasma-specific CD4+ T cell response that should be considered in testing next-generation vaccines against toxoplasmosis. Our results also are cautionary that individual vaccine constituents can cause severe harm depending on the company they keep.

Funder

National Institute of Allergy and Infectious Diseases of the National Institutes of Health

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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