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Cellular immunity in COVID-19 and other infections in Common variable immunodeficiency
Ragnhild Øye Løken1, Børre Fevang1,2
1Section of Clinical Immunology and Infectious Diseases, Division of Surgery, Inflammatory Medicine and Transplantation, Oslo University Hospital, Oslo, Norway.
Insights
Common variable immunodeficiency (CVID) patients show cellular immunity to COVID-19 and vaccines, despite impaired antibody production. Research is needed on optimal COVID-19 vaccine boosting schedules for CVID.
Area of Science:
- Immunology
- Virology
- Genetics
Background:
- Common variable immunodeficiency (CVID) involves impaired humoral immunity and T-cell dysregulation.
- The role of T-cell dysregulation in cellular immunity within CVID, especially concerning COVID-19, requires clarification.
Purpose of the Study:
- To review and summarize the existing literature on cellular immunity in CVID patients.
- To specifically focus on the impact of COVID-19 on cellular immunity in this population.
Main Methods:
- Literature review of studies on CVID, cellular immunity, and COVID-19.
- Analysis of T-cell responses to SARS-CoV-2 infection and vaccination in CVID patients.
Main Results:
- CVID patients generally exhibit a significant T-cell response to COVID-19 and mRNA vaccines, independent of antibody levels.
- Cellular immune responses wane over time but can be boosted, and opportunistic infections are rare.
- Influenza vaccine responses in CVID patients are comparable to healthy individuals, supporting annual vaccination.
Conclusions:
- CVID patients maintain cellular immunity against COVID-19 and respond to vaccination, though responses may be impaired.
- Further research is essential to determine optimal COVID-19 vaccine booster timing for CVID patients.
Abstract:
COVID-19 has shed light on the role of cellular immunity in the absence of humoral response in different patient groups. Common variable immunodeficiency (CVID) is characterized by impaired humoral immunity but also an underlying T-cell dysregulation. The impact of T-cell dysregulation on cellular immunity in CVID is not clear, and this review summarizes available literature on cellular immunity in CVID with a particular focus on COVID-19. Overall mortality of COVID-19 in CVID is difficult to assess, but seems not significantly elevated, and risk factors for severe disease mirrors that of the general population, including lymphopenia. Most CVID patients have a significant T-cell response to COVID-19 disease with possible cross-reactivity to endemic coronaviruses. Several studies find a significant but impaired cellular response to basal COVID-19 mRNA vaccination that is independent of an antibody response. CVID patients with infection only have better cellular responses to vaccine in one study, but there is no clear association to T-cell dysregulation. Cellular response wane over time but responds to a third booster dose of vaccine. Opportunistic infection as a sign of impaired cellular immunity in CVID is rare but is related to the definition of the disease. CVID patients have a cellular response to influenza vaccine that in most studies is comparable to healthy controls, and annual vaccination against seasonal influenza should be recommended. More research is required to clarify the effect of vaccines in CVID with the most immediate issue being when to booster the COVID-19 vaccine.
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