Immunogenicity and Tolerance of BNT162b2 mRNA Vaccine in Allogeneic Hematopoietic Stem Cell Transplant Patients

Author:

Ben Khlil Ahmed Amine12,Zamali Imen123ORCID,Belloumi Dorra24,Gdoura Mariem56ORCID,Kharroubi Ghassen237,Marzouki Soumaya3,Dachraoui Rym24,Ben Yaiche Insaf24,Bchiri Soumaya3,Hamdi Walid1,Gharbi Manel5,Ben Hmid Ahlem123,Samoud Samar13,Galai Yousr16,Torjmane Lamia24,Ladeb Saloua24,Bettaieb Jihene237,Triki Henda25,Ben Abdeljelil Nour24,Ben Othman Tarek24,Ben Ahmed Melika123ORCID

Affiliation:

1. Department of Clinical Immunology, Institut Pasteur de Tunis, Tunis 1002, Tunisia

2. Faculté de Médecine de Tunis, Université Tunis El Manar, Tunis 1068, Tunisia

3. Laboratory of Transmission, Control and Immunobiology of Infections (LR16IPT02), Institut Pasteur de Tunis, Tunis 1002, Tunisia

4. Department of Hematology and Transplant, Centre National de Greffe de Moelle Osseuse, Tunis 1006, Tunisia

5. Laboratory of Virology, Institut Pasteur de Tunis, Tunis 1002, Tunisia

6. Faculty of Pharmacy, University of Monastir, Monastir 5000, Tunisia

7. Department of Medical Epidemiology, Institut Pasteur de Tunis, Tunis 1002, Tunisia

Abstract

Background: Allogeneic hematopoietic stem cell transplantation (ASCT) induces acquired immunodeficiency, potentially altering vaccine response. Herein, we aimed to explore the clinical tolerance and the humoral and cellular immune responses following anti-SARS-CoV-2 vaccination in ASCT recipients. Methods: A prospective, non-randomized, controlled study that involved 43 ASCT subjects and 31 healthy controls. Humoral response was investigated using the Elecsys® test anti-SARS-CoV-2. Cellular response was assessed using the QFN® SARS-CoV-2 test. The lymphocyte cytokine profile was tested using the LEGENDplex™ HU Th Cytokine Panel Kit (12-plex). Results: Adverse effects (AE) were observed in 69% of patients, encompassing pain at the injection site, fever, asthenia, or headaches. Controls presented more side effects like pain in the injection site and asthenia with no difference in the overall AE frequency. Both groups exhibited robust humoral and cellular responses. Only the vaccine transplant delay impacted the humoral response alongside a previous SARS-CoV-2 infection. Noteworthily, controls displayed a Th1 cytokine profile, while patients showed a mixed Th1/Th2 profile. Conclusions: Pfizer-BioNTech® anti-SARS-CoV-2 vaccination is well tolerated in ASCT patients, inducing robust humoral and cellular responses. Further exploration is warranted to understand the impact of a mixed cytokine profile in ASCT patients.

Funder

Institute Pasteur of Tunis

Publisher

MDPI AG

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