Predictors of impaired antibody response after SARS-CoV-2 mRNA vaccination in hematopoietic cell transplant recipients: A Japanese multicenter observational study.


Journal

American journal of hematology
ISSN: 1096-8652
Titre abrégé: Am J Hematol
Pays: United States
ID NLM: 7610369

Informations de publication

Date de publication:
01 2023
Historique:
revised: 07 10 2022
received: 16 08 2022
accepted: 12 10 2022
pubmed: 20 10 2022
medline: 23 12 2022
entrez: 19 10 2022
Statut: ppublish

Résumé

HCT recipients reportedly have a high mortality rate after developing COVID-19. SARS-CoV-2 vaccination is generally useful to prevent COVID-19. However, its safety and efficacy among HCT recipients remain elusive. This large-scale prospective observational study including 543 HCT recipients with 37-months interval from transplant demonstrated high safety profiles of mRNA vaccine: only 0.9% of patients avoided the second dose due to adverse event or GVHD aggravation following the first dose. Regarding the efficacy, serological response with a clinically relevant titer (≥250 BAU/mL) was obtained in 397 (73.1%) patients. We classified the remaining 146 patients as impaired responders and compared the clinical and immunological parameters between two groups. In allogeneic HCT recipients, multivariable analysis revealed the risk factors for impaired serological response as follows: age (≥60, 1 points), HLA-mismatched donor (1 points), use of systemic steroids (1 points), absolute lymphocyte counts (<1000/μL, 1 points), absolute B-cell counts (<100/μL, 1 points), and serum IgG level (<500 mg/dL, 2 points). Notably, the incidence of impaired serological response increased along with the risk scores: patients with 0, 1-3, and 4-7 points were 3.9%, 21.8%, and 74.6%, respectively. In autologous HCT recipients, a shorter interval from transplant to vaccination was the only risk factor for impaired serological response. Our findings indicate that two doses of SARS-CoV-2 vaccine are safe but insufficient for a part of HCT recipients with higher risk scores. To improve this situation, we should consider additional treatment options, including booster vaccination and prophylactic neutralizing antibodies during the SARS-CoV-2 pandemic.

Identifiants

pubmed: 36260658
doi: 10.1002/ajh.26769
pmc: PMC9874814
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
RNA, Messenger 0

Types de publication

Observational Study Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102-111

Informations de copyright

© 2022 Wiley Periodicals LLC.

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Auteurs

Yasuo Mori (Y)

Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, Fukuoka, Japan.

Naoyuki Uchida (N)

Department of Hematology, Toranomon Hospital, Tokyo, Japan.

Takuya Harada (T)

Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, Fukuoka, Japan.

Yuta Katayama (Y)

Department of Hematology, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital, Hiroshima, Japan.

Atsushi Wake (A)

Department of Hematology, Toranomon Hospital Kajigaya, Kawasaki, Japan.

Hiromi Iwasaki (H)

Departments of Hematology, National Hospital Organization, Kyushu Medical Center, Fukuoka, Japan.

Tetsuya Eto (T)

Department of Hematology, Hamanomachi Hospital, Fukuoka, Japan.

Satoshi Morishige (S)

Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.

Tomoaki Fujisaki (T)

Department of Internal Medicine, Matsuyama Red Cross Hospital, Matsuyama, Japan.

Yoshikiyo Ito (Y)

Department of Hematology, Imamura General Hospital, Kagoshima, Japan.

Tomohiko Kamimura (T)

Department of Hematology, Harasanshin Hospital, Fukuoka, Japan.

Tsutomu Takahashi (T)

Department of Hematology, Shimane University Hospital, Izumo, Japan.

Yutaka Imamura (Y)

Division of Hematology, St. Mary's Hospital, Kurume, Japan.

Kazushi Tanimoto (K)

Department of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, Ehime, Japan.

Kenji Ishitsuka (K)

Department of Hematology and Rheumatology, Kagoshima University Hospital, Kagoshima, Japan.

Junichi Sugita (J)

Department of Hematology, Hokkaido University Hospital, Sapporo, Japan.

Noriaki Kawano (N)

Department of Internal Medicine, Miyazaki Prefectural Miyazaki Hospital, Miyazaki, Japan.

Kazuki Tanimoto (K)

Department of Hematology, Fukuoka Red Cross Hospital, Fukuoka, Japan.

Goichi Yoshimoto (G)

Department of Hematology, Saga-Ken Medical Center Koseikan, Saga, Japan.

Ilseung Choi (I)

Department of Hematology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.

Tomonori Hidaka (T)

Department of Gastroenterology and Hematology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

Ryosuke Ogawa (R)

Department of Hematology and Oncology, JCHO Kyushu Hospital, Fukuoka, Japan.

Yasushi Takamatsu (Y)

Division of Medical Oncology, Hematology and Infectious Diseases, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Toshihiro Miyamoto (T)

Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, Fukuoka, Japan.
Division of Hematology, Faculty of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.

Koichi Akashi (K)

Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, Fukuoka, Japan.

Koji Nagafuji (K)

Division of Hematology and Oncology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.

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