Patients with Chronic Lymphocytic Leukemia Have a Very High Risk of Ineffective Response to the BNT162b2 Vaccine.

COVID-19 chronic lymphocytic leukemia (CLL) hypogammaglobulinemia immunity immunocompromised vaccine

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
21 Jul 2022
Historique:
received: 18 06 2022
revised: 15 07 2022
accepted: 19 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

Patients with CLL have high rates of either severe disease or death from COVID-19 and a low response rate after COVID-19 vaccination has been reported. We conducted a single-center study with the main objective to evaluate the immunogenicity of the BNT1162b2 mRNA vaccines in 42 patients affected by CLL with the assessment of antibody response after the second and the third dose. After the second dose of vaccine, 13 patients (30%) showed an antibody response. The presence of hypogammaglobulinemia and the use of steroids or IVIG were the main factors associated with poor response. After the third dose, 5/27 (18%) patients showed an antibody response while in non-responders to the second dose, only 1 patient (4%) showed an elicitation of the immune response by the third dose, with no statistically significant difference. Our data, despite the small size of our cohort, demonstrate that patients with CLL have a low rate of effective response to the BNT162b2 vaccine. However, the effective role of a subsequent dose is still unclear, highlighting the need for alternative methods of immunization in this particularly fragile group of patients.

Identifiants

pubmed: 35891328
pii: vaccines10071162
doi: 10.3390/vaccines10071162
pmc: PMC9317769
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Andrea Galitzia (A)

Department of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.

Luca Barabino (L)

Department of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.

Roberta Murru (R)

Hematology and Transplant Centre, Ospedale Oncologico Armando Businco, ARNAS G. Brotzu, 09121 Cagliari, Italy.

Giovanni Caocci (G)

Department of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.
Hematology and Transplant Centre, Ospedale Oncologico Armando Businco, ARNAS G. Brotzu, 09121 Cagliari, Italy.

Marianna Greco (M)

Hematology and Transplant Centre, Ospedale Oncologico Armando Businco, ARNAS G. Brotzu, 09121 Cagliari, Italy.

Giancarlo Angioni (G)

Laboratory of Clinical Chemical Analysis and Microbiology, ARNAS G. Brotzu, 09134 Cagliari, Italy.

Olga Mulas (O)

Department of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.
Hematology and Transplant Centre, Ospedale Oncologico Armando Businco, ARNAS G. Brotzu, 09121 Cagliari, Italy.

Sara Oppi (S)

Hematology and Transplant Centre, Ospedale Oncologico Armando Businco, ARNAS G. Brotzu, 09121 Cagliari, Italy.

Stefania Massidda (S)

Hematology and Transplant Centre, Ospedale Oncologico Armando Businco, ARNAS G. Brotzu, 09121 Cagliari, Italy.

Alessandro Costa (A)

Department of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.

Giorgio La Nasa (G)

Department of Medical Sciences and Public Health, University of Cagliari, 09042 Monserrato, Italy.
Hematology and Transplant Centre, Ospedale Oncologico Armando Businco, ARNAS G. Brotzu, 09121 Cagliari, Italy.

Classifications MeSH