Immunocompromised Pediatric Patients Showed T-cell Activity and Humoral Immunity Against SARS-CoV-2
According to data from a recent study of adult and pediatric patients with antibody deficiencies, patients that often fail to make protective immune responses to infections and vaccinations showed robust T-cell activity and humoral immunity against SARS-CoV-2 structural proteins.
The new study published on May 13, 2021, led by researchers at Children’s National Hospital, is the first to demonstrate a robust T-cell response against SARS-CoV-2 in immunocompromised patients.
The study, published in the Journal of Clinical Immunology, showed that patients with antibody deficiency disorders, including inborn errors of immunity (IEI) and common variable immunodeficiency (CVID), can mount an immune response to SARS-CoV-2.
The findings propose that COVID-19 vaccination may still be helpful for this population, said these researchers.
“If T-cell responses to SARS-CoV-2 are indeed protective, then it could suggest that adoptive T-cell immunotherapy might benefit more profoundly immunocompromised patients,” stated Michael Keller, M.D., director of the Translational Research Laboratory in the Program for Cell Enhancement and Technologies for Immunotherapy at Children’s National, located in Washington DC, in a related press statement.
“Through our developing phase I study T-cell immunotherapy protocol, we intend to investigate if coronavirus-specific T-cells may be protective following bone marrow transplantation, as well as in other immunodeficient populations.”
“This data suggests that many patients with antibody deficiency should be capable of responding to COVID-19 vaccines, and current studies at the National Institutes of Health and elsewhere are addressing whether those responses are likely to be protective and lasting,” added Dr. Keller.
The T-cell responses in all the COVID-19 patients were similar in magnitude to healthy adult and pediatric convalescent participants.
Currently, there is very little data on adaptive immune responses to SARS-CoV-2 in these vulnerable populations.
The study sheds light on the antibody and T-cell responses to SARS-CoV-2 protein spikes based on a sample size of six patients, including a family group of three children and their mother. All have antibody deficiencies and developed mild COVID-19 symptoms, minus one child who remained asymptomatic.
Control participants were the father of the same family, who tested positive for COVID-19, and another incidental adult (not next of kin) experienced mild COVID-19 symptoms. The researchers took blood samples to test the T-cell response in cell cultures and provided comprehensive statistical analysis of the adaptive immune responses.
“This was a small group of patients, but given the high proportion of responses, it does suggest that many of our antibody deficient patients are likely to mount immune responses to SARS-CoV-2.”
“Additional studies are needed to know whether other patients with primary immunodeficiency develop immunity following COVID-19 infection and will likely be answered by a large international collaboration organized by our collaborators at the Garvan Institute in Sydney,” concluded Dr. Keller.
Previously, anticipating an expanded use authorization by the U.S. Food and Drug Administration (FDA), Children’s National Hospital established a waitlist for children ages 12 and up on May 5, 2021. The FDA announced the expanded authorization on May 10th.
Children’s National Hospital has vaccinated close to 4,000 adolescents since December 2020. Children’s National Hospital celebrates 150 years of pediatric care, research, and commitment to the community.
PrecisionVaccinations publishes research-based vaccine news.
- Robust Antibody and T Cell Responses to SARS-CoV-2 in Patients with Antibody Deficiency
- Coronavirus disease 2019 in patients with inborn errors of immunity: An international study
- Children’s National opens vaccine waitlist for children 12 and up in anticipation of Pfizer authorization
- U.S. FDA Authorizes mRNA COVID-19 Vaccine for Adolescents