Humoral immune response and serological profile of autoantibodies in heart transplant recipients after vaccination against coronavirus infection.

Due to the mandatory immunosuppression and concomitant diseases, heart transplant recipients are at an increased risk of an adverse outcome from COVID-19 infection. The efficacy and safety of using vaccines to prevent COVID-19 infection in patients with heart transplants, including the development of undesirable inflammatory and autoimmune reactions, has not been sufficiently studied. This paper presents the characteristics of humoral immunity and the analysis of autoantibody production in heart transplant recipients after vaccination against a coronavirus infection. The main group consisted of patients (n = 40) who underwent orthotopic heart transplantation in the period from 2009 to 2021 at the National Research and Practical Center “Cardiology” and received two doses of the Vero Cell vaccine (China) or got a three-step booster Gam-COVID-Vac (Sputnik V, Russian Federation). It has been shown that 63 % of vaccinated individuals with no previous COVID-19 history and 85 % of patients with a history of COVID-19 infection developed humoral post-vaccination immunity. The humoral response in patients who had seroconversion prior to vaccination exhibited elevated levels of virusspecific IgG antibodies to the SARS-CoV-2 virus S protein during the post-vaccination period, with a statistically significant increase observed by 9–12 months after booster vaccination. Vaccination against the coronavirus infection does not result in an increase of serum autoantibodies (RF IgG and IgA, anti-SSR, cardiolipin IgG, β2-glycoprotein IgG, ANA, ANCA-Pro, anti-SLA/LP, anti-GD-IgA) in heart transplant recipients. At the same time, vaccinated heart transplant recipients with a history of coronavirus infection showed an increase in the level of antibodies to IFN-α for a period of 9–12 months after the main vaccination. This evidence, when associated with HLA alleles, must be taken into account for identifying patients who may be at risk of developing severe diseases.

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Journal
Doklady of the National Academy of Sciences of Belarus
Published
2025-08-28
DOI
https://doi.org/10.29235/1561-8323-2025-69-4-303-313
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
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article

Humoral immune response and serological profile of autoantibodies in heart transplant recipients after vaccination against coronavirus infection.

M. G. Kolyadko, Irina Russkih, D. B. Nizheharodava, G. I. Ivanchyk et al.
Doklady of the National Academy of Sciences of Belarus
SARS-CoV-2 and COVID-19 Research
article

Humoral immune response and serological profile of autoantibodies in heart transplant recipients after vaccination against coronavirus infection.

M. G. Kolyadko, Irina Russkih, D. B. Nizheharodava, G. I. Ivanchyk, M. М. Zafranskayа, Alesia V. Vialichka, E. K. Kurlyanskaya, О. Г. Шатова, Elizaveta M. Nazaranka
article en

Abstract

Due to the mandatory immunosuppression and concomitant diseases, heart transplant recipients are at an increased risk of an adverse outcome from COVID-19 infection. The efficacy and safety of using vaccines to prevent COVID-19 infection in patients with heart transplants, including the development of undesirable inflammatory and autoimmune reactions, has not been sufficiently studied. This paper presents the characteristics of humoral immunity and the analysis of autoantibody production in heart transplant recipients after vaccination against a coronavirus infection. The main group consisted of patients (n = 40) who underwent orthotopic heart transplantation in the period from 2009 to 2021 at the National Research and Practical Center “Cardiology” and received two doses of the Vero Cell vaccine (China) or got a three-step booster Gam-COVID-Vac (Sputnik V, Russian Federation). It has been shown that 63 % of vaccinated individuals with no previous COVID-19 history and 85 % of patients with a history of COVID-19 infection developed humoral post-vaccination immunity. The humoral response in patients who had seroconversion prior to vaccination exhibited elevated levels of virusspecific IgG antibodies to the SARS-CoV-2 virus S protein during the post-vaccination period, with a statistically significant increase observed by 9–12 months after booster vaccination. Vaccination against the coronavirus infection does not result in an increase of serum autoantibodies (RF IgG and IgA, anti-SSR, cardiolipin IgG, β2-glycoprotein IgG, ANA, ANCA-Pro, anti-SLA/LP, anti-GD-IgA) in heart transplant recipients. At the same time, vaccinated heart transplant recipients with a history of coronavirus infection showed an increase in the level of antibodies to IFN-α for a period of 9–12 months after the main vaccination. This evidence, when associated with HLA alleles, must be taken into account for identifying patients who may be at risk of developing severe diseases.

Doklady of the National Academy of Sciences of BelarusVol. 69(4)
Belarusian State University (BY), Scientific Research Institute of Experimental and Clinical Medicine (RU), Republican Scientific and Practical Center of Neurology and Neurosurgery (BY), International Sakharov Environmental Institute (BY), Belarusian State Medical University (BY)
Openalex Percentile: Top 72%
SARS-CoV-2 and COVID-19 Research
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