Reconstitution of Norovirus-Specific T-Cell Responses Following Hematopoietic Stem Cell Transplantation in Patients With Inborn Errors of Immunity and Chronic Norovirus Infection

Author:

Durkee-Shock Jessica1ORCID,Cohen Ariella2,Maghzian Naseem2,Pezzella Gloria2,Jensen-Wachspress Mariah2,Hostal Anna1,Barton Karenna1,Gangler Krista1,Dávila Saldaña Blachy J23,Chaimongkol Natthawan1,Bollard Catherine M23,Sosnovtsev Stanislav V1,Cohen Jeffrey1,Nagata Bianca M4,Alves Derron A4,Ghosh Rajarshi5,Seifert Bryce A5,Freeman Alexandra6,Gonzalez Corina7,Notarangelo Luigi D6,Green Kim Y1,Keller Michael D28

Affiliation:

1. Laboratory of Infectious Diseases, Division of Intramural Research, National Institute of Allergy and Infectious Diseases , Bethesda, Maryland

2. Center for Cancer and Immunology Research, Children’s National Hospital , Washington, District of Columbia

3. Division of Blood and Marrow Transplantation, Children’s National Hospital , Washington, District of Columbia

4. Infectious Disease Pathogenesis Section, Division of Intramural Research, National Institute of Allergy and Infectious Diseases , Rockville, Maryland

5. NIAID Centralized Sequencing Program, Division of Intramural Research, National Institute of Allergy and Infectious Diseases , Bethesda, Maryland

6. Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases , Bethesda, Maryland

7. Immune Deficiency Cellular Therapy Program, National Cancer Institute , Bethesda, Maryland

8. Division of Allergy and Immunology, Children's National Hospital , Washington, District of Columbia

Abstract

Abstract Background Chronic norovirus infection (CNI) causes significant morbidity in immunocompromised patients. No effective prevention or treatment currently exists. Methods Two patients with inborn errors of immunity, X-linked severe combined immunodeficiency (X-SCID) and DOCK8 deficiency, were followed longitudinally for clinical course, immune reconstitution, norovirus-specific T-cell (NST) response, B-cell reconstitution, and norovirus-specific antibody production. Samples were obtained in the peri-hematopoietic stem cell transplant (HSCT) setting before and after CNI clearance. The norovirus strain causing CNI was followed longitudinally for norovirus stool viral loads and sequencing. Results The noroviruses were identified as GII.4 Sydney[P4 New Orleans] in 1 patient and GII.17[P17] in the other. An exacerbation of diarrhea post-HSCT in the patient with X-SCID was consistent with norovirus infection but not with graft-versus-host disease on pathologic samples. Both patients recovered polyfunctional NSTs in the CD4 and CD8 T-cell compartments that recognized multiple norovirus structural and nonstructural viral antigens. T-cell responses were minimal during active CNI but detectable after resolution. Mapping of NST responses between the patient with DOCK8 deficiency and his matched sibling donor were nearly identical. B-cell reconstitution or new endogenous antibody production for immunoglobulin A or immunoglobulin G was not observed. Conclusions This report is the first to demonstrate reconstitution of NST immunity after HSCT closely temporally aligned with clearance of CNI, suggesting that cellular immunity is sufficient for norovirus clearance.

Funder

National Heart, Lung, and Blood Institute

Jeffrey Modell Foundation

Publisher

Oxford University Press (OUP)

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