Attenuated immunogenicity of SARS-CoV-2 vaccines and risk factors in stem cell transplant recipients: a meta-analysis.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
26 09 2023
Historique:
accepted: 25 06 2023
received: 03 04 2023
medline: 19 9 2023
pubmed: 30 6 2023
entrez: 30 6 2023
Statut: ppublish

Résumé

Immunogenicity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination is diminished in hematopoietic stem cell transplant (HSCT) recipients. To summarize current evidence and identify risk factors for attenuated responses, 5 electronic databases were searched since database inceptions through 12 January 2023 for studies reporting humoral and/or cellular immunogenicity of SARS-CoV-2 vaccination in the HSCT population. Using descriptive statistics and random-effects models, extracted numbers of responders and pooled odds ratios (pORs) with 95% confidence intervals (CIs) for risk factors of negative immune responses were analyzed (PROSPERO: CRD42021277109). From 61 studies with 5906 HSCT recipients, after 1, 2, and 3 doses of messenger RNA (mRNA) SARS-CoV-2 vaccines, the mean antispike antibody seropositivity rates (95% CI) were 38% (19-62), 81% (77-84), and 80% (75-84); neutralizing antibody seropositivity rates were 52% (40-64), 71% (54-83), and 78% (61-89); and cellular immune response rates were 52% (39-64), 66% (51-79), and 72% (52-86). After 2 vaccine doses, risk factors (pOR; 95% CI) associated with antispike seronegativity were male recipients (0.63; 0.49-0.83), recent rituximab exposure (0.09; 0.03-0.21), haploidentical allografts (0.46; 0.22-0.95), <24 months from HSCT (0.25; 0.07-0.89), lymphopenia (0.18; 0.13-0.24), hypogammaglobulinemia (0.23; 0.10-0.55), concomitant chemotherapy (0.48; 0.29-0.78) and immunosuppression (0.18; 0.13-0.25). Complete remission of underlying hematologic malignancy (2.55; 1.05-6.17) and myeloablative conditioning (1.72; 1.30-2.28) compared with reduced-intensity conditioning were associated with antispike seropositivity. Ongoing immunosuppression (0.31; 0.10-0.99) was associated with poor cellular immunogenicity. In conclusion, attenuated humoral and cellular immune responses to mRNA SARS-CoV-2 vaccination are associated with several risk factors among HSCT recipients. Optimizing individualized vaccination and developing alternative COVID-19 prevention strategies are warranted.

Identifiants

pubmed: 37389818
pii: 496657
doi: 10.1182/bloodadvances.2023010349
pmc: PMC10514108
doi:

Substances chimiques

COVID-19 Vaccines 0
Antibodies, Neutralizing 0

Types de publication

Meta-Analysis Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5624-5636

Informations de copyright

© 2023 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

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Auteurs

Tanaporn Meejun (T)

Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Karan Srisurapanont (K)

Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.

Kasama Manothummetha (K)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

Achitpol Thongkam (A)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Nuthchaya Mejun (N)

Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Nipat Chuleerarux (N)

Department of Medicine, University of Miami/Jackson Memorial Hospital, Miami, FL.

Anawin Sanguankeo (A)

Department of Preventive and Social Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Kasidis Phongkhun (K)

Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.

Surachai Leksuwankun (S)

Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.

Jaedvara Thanakitcharu (J)

Faculty of Medicine, Srinakharinwirot University, Nakhon Nayok, Thailand.

Bhoowit Lerttiendamrong (B)

Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Nattapong Langsiri (N)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Pattama Torvorapanit (P)

Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
Thai Red Cross Emerging Infectious Diseases Clinical Center, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.

Navaporn Worasilchai (N)

Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand.

Rongpong Plongla (R)

Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.

Nattiya Hirankarn (N)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Saman Nematollahi (S)

Department of Medicine, University of Arizona College of Medicine, Tucson, AZ.

Nitipong Permpalung (N)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Chatphatai Moonla (C)

Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
Center of Excellence in Translational Hematology, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Bangkok, Thailand.

Olivia S Kates (OS)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.

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