Sutimlimab suppresses SARS-CoV-2 mRNA vaccine-induced hemolytic crisis in a patient with cold agglutinin disease.

cold agglutinin disease severe acute respiratory syndrome coronavirus 2 sutimlimab

Journal

Journal of clinical and experimental hematopathology : JCEH
ISSN: 1880-9952
Titre abrégé: J Clin Exp Hematop
Pays: Japan
ID NLM: 101141257

Informations de publication

Date de publication:
2023
Historique:
medline: 27 12 2023
pubmed: 27 12 2023
entrez: 26 12 2023
Statut: ppublish

Résumé

Cold agglutinin disease (CAD) is a rare form of acquired autoimmune hemolytic anemia driven mainly by antibodies that activate the classical complement pathway. Several patients with CAD experience its development or exacerbation of hemolysis after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or after receiving the SARS-CoV-2 mRNA vaccine. Therefore, these patients cannot receive an additional SARS-CoV-2 mRNA vaccination and have a higher risk of severe SARS-CoV-2 infection. Sutimlimab is a monoclonal antibody that inhibits the classical complement pathway of the C1s protein and shows rapid and sustained inhibition of hemolysis in patients with CAD. However, whether sutimlimab could also inhibit hemolysis caused by SARS-CoV-2 mRNA vaccination is uncertain. Here, we present the case of a 70-year-old man with CAD who repeatedly experienced a hemolytic crisis after receiving SARS-CoV-2 mRNA vaccines. The patient eventually underwent SARS-CoV-2 mRNA vaccination safely, without hemolytic attack, under classical pathway inhibition therapy with sutimlimab. This report suggests that appropriate sutimlimab administration can suppress SARS-CoV-2 mRNA vaccination-induced CAD exacerbation, and that it could be a preventive strategy to minimize hemolytic attacks in susceptible populations.

Identifiants

pubmed: 38148014
doi: 10.3960/jslrt.23040
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

246-250

Auteurs

Hiroki Kobayashi (H)

Department of Internal Medicine, Tsuyama Chuo Hospital, Okayama, Japan.
Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Tomoki Ouchi (T)

Department of Internal Medicine, Tsuyama Chuo Hospital, Okayama, Japan.

Wataru Kitamura (W)

Department of Hematology, Oncology and Respiratory Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

Shoji Asakura (S)

Department of Internal Medicine, Okayama Rosai Hospital, Okayama, Japan.

Tomofumi Yano (T)

Department of Internal Medicine, Okayama Rosai Hospital, Okayama, Japan.

Hiromasa Takeda (H)

Department of Internal Medicine, Tsuyama Chuo Hospital, Okayama, Japan.

Yoshiyuki Tokuda (Y)

Department of Internal Medicine, Tsuyama Chuo Hospital, Okayama, Japan.

Tadashi Yoshino (T)

Department of Pathology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

Yoshinobu Maeda (Y)

Department of Hematology, Oncology, and Respiratory Medicine, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

Classifications MeSH