TY - JOUR
T1 - Development of Potent Cellular and Humoral Immune Responses in Long-Term Hemodialysis Patients After 1273-mRNA SARS-CoV-2 Vaccination
AU - Gonzalez-Perez, Maria
AU - Montes-Casado, Maria
AU - Conde, Patricia
AU - Cervera, Isabel
AU - Baranda, Jana
AU - Berges-Buxeda, Marcos J.
AU - Perez-Olmeda, Mayte
AU - Sanchez-Tarjuelo, Rodrigo
AU - Utrero-Rico, Alberto
AU - Lozano-Ojalvo, Daniel
AU - Torre, Denis
AU - Schwarz, Megan
AU - Guccione, Ernesto
AU - Camara, Carmen
AU - Llópez-Carratalá, M. Rosario
AU - Gonzalez-Parra, Emilio
AU - Portoles, Pilar
AU - Ortiz, Alberto
AU - Portoles, Jose
AU - Ochando, Jordi
N1 - Funding Information:
Funding was obtained from Instituto de Salud Carlos III (ISCIII) RICORS program to RICORS2040 (RD21/0005/0001), FEDER funds; Acción Estratégica en Salud Intramural (AESI), Instituto de Salud Carlos III, grant number AESI PI21CIII_00022 to PP and Healthstar-plus -REACT-UE Grant through Segovia Arana Research Institute Puerta de Hierro Majadahonda-IDIPHIM. JO is a member of VACCELERATE (European Corona Vaccine Trial Accelerator Platform) Network, which aims to facilitate and accelerate the design and implementation of COVID-19 phase 2 and 3 vaccine trials. JO is a member of the INsTRuCT under the MSC grant agreement Nº860003 (Innovative Training in Myeloid Regulatory Cell Therapy) Consortium, a network of European scientists from academia and industry focused on developing innovative immunotherapies.
Funding Information:
We thank Mar?a Castillo-de la Osa (PEJ2018-004557-A) for technical assistance.
Publisher Copyright:
Copyright © 2022 Gonzalez-Perez, Montes-Casado, Conde, Cervera, Baranda, Berges-Buxeda, Perez-Olmeda, Sanchez-Tarjuelo, Utrero-Rico, Lozano-Ojalvo, Torre, Schwarz, Guccione, Camara, Llópez-Carratalá, Gonzalez-Parra, Portoles, Ortiz, Portoles and Ochando.
PY - 2022/3/23
Y1 - 2022/3/23
N2 - Long-term hemodialysis (HD) patients are considered vulnerable and at high-risk of developing severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) infection due to their immunocompromised condition. Since COVID-19 associated mortality rates are higher in HD patients, vaccination is critical to protect them. The response towards vaccination against COVID-19 in HD patients is still uncertain and, in particular the cellular immune response is not fully understood. We monitored the humoral and cellular immune responses by analysis of the serological responses and Spike-specific cellular immunity in COVID-19-recovered and naïve HD patients in a longitudinal study shortly after vaccination to determine the protective effects of 1273-mRNA vaccination against SARS-CoV-2 in these high-risk patients. In naïve HD patients, the cellular immune response measured by IL-2 and IFN-ɣ secretion needed a second vaccine dose to significantly increase, with a similar pattern for the humoral response. In contrast, COVID-19 recovered HD patients developed a potent and rapid cellular and humoral immune response after the first vaccine dose. Interestingly, when comparing COVID-19 recovered healthy volunteers (HV), previously vaccinated with BNT162b2 vaccine to HD patients vaccinated with 1273-mRNA, these exhibited a more robust immune response that is maintained longitudinally. Our results indicate that HD patients develop strong cellular and humoral immune responses to 1273-mRNA vaccination and argue in favor of personalized immune monitoring studies in HD patients, especially if COVID-19 pre-exposed, to adapt COVID-19 vaccination protocols for this immunocompromised population.
AB - Long-term hemodialysis (HD) patients are considered vulnerable and at high-risk of developing severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) infection due to their immunocompromised condition. Since COVID-19 associated mortality rates are higher in HD patients, vaccination is critical to protect them. The response towards vaccination against COVID-19 in HD patients is still uncertain and, in particular the cellular immune response is not fully understood. We monitored the humoral and cellular immune responses by analysis of the serological responses and Spike-specific cellular immunity in COVID-19-recovered and naïve HD patients in a longitudinal study shortly after vaccination to determine the protective effects of 1273-mRNA vaccination against SARS-CoV-2 in these high-risk patients. In naïve HD patients, the cellular immune response measured by IL-2 and IFN-ɣ secretion needed a second vaccine dose to significantly increase, with a similar pattern for the humoral response. In contrast, COVID-19 recovered HD patients developed a potent and rapid cellular and humoral immune response after the first vaccine dose. Interestingly, when comparing COVID-19 recovered healthy volunteers (HV), previously vaccinated with BNT162b2 vaccine to HD patients vaccinated with 1273-mRNA, these exhibited a more robust immune response that is maintained longitudinally. Our results indicate that HD patients develop strong cellular and humoral immune responses to 1273-mRNA vaccination and argue in favor of personalized immune monitoring studies in HD patients, especially if COVID-19 pre-exposed, to adapt COVID-19 vaccination protocols for this immunocompromised population.
KW - COVID-19
KW - SARS-CoV-2 vaccine
KW - cellular response
KW - chronic kidney disease
KW - hemodialysis
KW - humoral response
UR - http://www.scopus.com/inward/record.url?scp=85127921276&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2022.845882
DO - 10.3389/fimmu.2022.845882
M3 - Article
C2 - 35401504
AN - SCOPUS:85127921276
VL - 13
JO - Frontiers in Immunology
JF - Frontiers in Immunology
SN - 1664-3224
M1 - 845882
ER -