Response to anti-SARS-CoV-2 mRNA vaccines in multiple myeloma and chronic lymphocytic leukemia patients

Joanna Zaleska1,2, Paulina Kwasnik1, Magdalena Paziewska1

  • 1Department of Experimental Hematooncology, Medical University of Lublin, Lublin, Poland.

Insights

mRNA COVID-19 vaccines show improved antibody responses in multiple myeloma (MM) and chronic lymphocytic leukemia (CLL) patients. However, T-cell responses may not correlate with antibody levels in these immunocompromised individuals.

Area of Science:

  • Immunology
  • Oncology
  • Infectious Diseases

Background:

  • Patients with multiple myeloma (MM) and chronic lymphocytic leukemia (CLL) face higher risks from COVID-19 due to disease-related and treatment-induced immunosuppression.
  • This immune impairment also leads to reduced effectiveness of vaccinations in these populations.

Purpose of the Study:

  • To evaluate the humoral and T cell-mediated immune responses to mRNA COVID-19 vaccines (BNT162b2 or mRNA-1273) in patients with MM and CLL.
  • To assess these responses in both short-term (2-5 weeks) and long-term (12 weeks) follow-up periods after the second vaccine dose.

Main Methods:

  • Blood samples were collected from 62 CLL and 60 MM patients between March and August 2021 in Poland.
  • Detected total anti-RBD antibodies and quantified specific CD8+ T cells against SARS-CoV-2 before and after vaccination.

Main Results:

  • Anti-RBD antibody levels significantly increased post-vaccination in both MM (37% pre-vaccination to 91% short-term, 94% long-term) and CLL patients (21% pre-vaccination to 45% short-term, 71% long-term).
  • A trend towards increased CD8+ T cells against SARS-CoV-2 was observed in MM patients post-vaccination, but no significant changes were noted in CLL patients.
  • No positive correlation was found between vaccine-induced CD8+ T cell responses and serological antibody levels.

Conclusions:

  • mRNA COVID-19 vaccination elicits a notable humoral immune response in immunocompromised MM and CLL patients.
  • While T-cell responses may be induced, their correlation with antibody levels is not consistently observed, suggesting complex immune dynamics in these patient groups.

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