Persistent Immunity against SARS-CoV-2 in Individuals with Oncohematological Diseases Who Underwent Autologous or Allogeneic Stem Cell Transplantation after Vaccination

Author:

Rodríguez-Mora Sara12ORCID,Pérez-Lamas Lucía3ORCID,Sainero Miriam Solera1,Torres Montserrat12,Sánchez-Menéndez Clara134ORCID,Corona Magdalena34ORCID,Mateos Elena12,Casado-Fernández Guiomar14ORCID,Alcamí José25ORCID,García-Pérez Javier25ORCID,Pérez-Olmeda Mayte26ORCID,Murciano-Antón María Aranzazú7,López-Jiménez Javier3ORCID,García-Gutiérrez Valentín3ORCID,Coiras Mayte12ORCID

Affiliation:

1. Immunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, 28220 Madrid, Spain

2. Biomedical Research Center Network in Infectious Diseases (CIBERINFEC), Instituto de Salud Carlos III, 28029 Madrid, Spain

3. Hematology and Hemotherapy Service, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Hospital Universitario Ramón y Cajal, 28034 Madrid, Spain

4. Faculty of Sciences, Universidad de Alcalá, 28801 Madrid, Spain

5. AIDS Immunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, 28220 Madrid, Spain

6. Serology Service, Instituto de Salud Carlos III, 28029 Madrid, Spain

7. Family Medicine, Centro de Salud Doctor Pedro Laín Entralgo, 28924 Alcorcón, Spain

Abstract

The high morbimortality due to SARS-CoV-2 infection in oncohematological diseases (OHD) and hematopoietic stem cell transplant (HSCT) recipients in the pre-vaccine era has made vaccination a priority in this group. After HSCT, the immune responses against common vaccines such as tetanus, varicella, rubella, and polio may be lost. However, the loss of immunity developed by COVID-19 vaccination after HSCT has not been completely defined. In this study, both humoral and cellular immunity against SARS-CoV-2 were analyzed in 29 individuals with OHD who were vaccinated before receiving allogeneic (n = 11) or autologous (n = 18) HSCT. All participants had low but protective levels of neutralizing IgGs against SARS-CoV-2 after HSCT despite B-cell lymphopenia and immaturity. Although antibody-dependent cellular cytotoxicity was impaired, direct cellular cytotoxicity was similar to healthy donors in participants with autologous-HSCT, in contrast to individuals with allogeneic–HSCT, which severely deteriorated. No significant changes were observed in the immune response before and after HSCT. During follow-up, all reported post-HSCT SARS-CoV-2 infections were mild. This data emphasizes that COVID-19 vaccination is effective, necessary, and safe for individuals with OHD and also supports the persistence of some degree of immune protection after HSCT, at least in the short term, when patients cannot yet be revaccinated.

Funder

Instituto de Salud Carlos III

European Regional Development Fund

Coordinated Research Activities at the National Center of Microbiology

Chiesi España, S.A.U.

Spanish Ministry of Science and Innovation

NIH

CIBERINFEC

Programa Investigo, FIBio HRC-IRYCIS

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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