Cellular and Humoral Immune Responses after Breakthrough Infection in Patients Undergoing Hemodialysis
Year: 2023
Type: article
Study design: Observational Study
Abstract: Coronavirus disease 2019 (COVID-19) following primary immunization (breakthrough infection) has been reported in hemodialysis patients; however, their post-infection immune status remains unclear. We evaluated the humoral and cellular immunity of hemodialysis patients after breakthrough infection. Hemodialysis patients who had received primary immunization against COVID-19 at least six months prior to the study but developed mild/moderate COVID-19 before a booster dose (breakthrough infection group) and hemodialysis patients who were not infected with COVID-19 but received a booster dose (booster immunization group) were recruited. In both groups, SARS-CoV-2 antigen-specific cytokines and IgG levels were measured three weeks after infection or three weeks after receiving a booster dose. Memory T and B cells were also counted in the breakthrough infection group using flow cytometry three weeks after infection. Significantly higher SARS-CoV-2 antigen-specific IgG, IFN-γ, IL-5, TNF-α, and IL-6 levels occurred in the breakthrough infection group compared to the booster immunization group (p = 0.013, 0.039, 0.024, 0.017, and 0.039, respectively). The SARS-CoV-2 antigen-specific IgG and cytokine levels were not significantly different between the two groups. The breakthrough infection group had significantly higher percentages of central and effector memory T cells and regulatory T cells than the comparison group (p = 0.008, 0.031, and 0.026, respectively). Breakthrough infections may induce stronger cellular and humoral immune responses than booster immunizations in hemodialysis patients.
Source: Vaccines
Institutions: Saiseikai Central Hospital, Keio University, Kitasato University
Language: English
Subfield: Infectious Diseases
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,447
Awards: G1004945140, 変異に対応した新型コロナウイルス(SARS-CoV-2)に対する中和抗体の開発, 多様な前向きコホートを用いたCOVID-19ワクチンの多角的解析, G2200186691, G2261881054, 単剤で既存のVOC株全てに有効な第2世代SARS-CoV-2中和抗体の開発, G350838144, 新型コロナウイルス感染症の重症化阻止を目指した医薬品・次世代型ワクチン開発に必要な遺伝学・免疫学・代謝学的基盤研究の推進, Therapeutic approach to confer an anti-tumorigenic role of IL-6 to the pro-tumorigenic cytokine in effector T cells, G4496210335, G4525685779, G4822051657, G4933698494, G6086680785, 新型コロナ変異ウイルスに対する遺伝学的、免疫学的、代謝学的病態解明および治療戦略の策定, G6481698008, G7000503590, Brain inflammation and repair mechanism by adaptive immunity, G7390550691, G8113279118, 新型コロナウイルス(SARS-CoV-2)に対する中和抗体医薬の開発, G8941407038
OpenAlex ID: W4383535569
