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Cited 4 time in webofscience Cited 2 time in scopus
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Augmented humoral and cellular immunity against severe acute respiratory syndrome coronavirus 2 after breakthrough infection in kidney transplant recipients who received 3 doses of coronavirus disease 2019 vaccineopen access

Authors
Yang, J[Yang, Jinyoung]Lee, KW[Lee, Kyo Won]Baek, JY[Baek, Jin Yang]Bae, S[Bae, Seongman]Lee, YH[Lee, Young Ho]Kim, H[Kim, Haein]Huh, K[Huh, Kyungmin]Cho, SY[Cho, Sun Young]Kang, CI[Kang, Cheol-In]Chung, DR[Chung, Doo Ryeon]Peck, KR[Peck, Kyong Ran]Park, JB[Park, Jae Berm]Kim, SH[Kim, Sung -Han]Kim, TJ[Kim, Tae -Jong]Kim, DM[Kim, Dong-Min]Ko, JH[Ko, Jae-Hoon]
Issue Date
1-Apr-2023
Publisher
ELSEVIER SCIENCE INC
Keywords
breakthrough infection (BI); cellular immunity; humoral immunity; kidney transplant; severe acute respiratory syndrome coronavirus; 2 (SARS-CoV-2)
Citation
AMERICAN JOURNAL OF TRANSPLANTATION, v.23, no.4, pp.565 - 572
Indexed
SCIE
SCOPUS
Journal Title
AMERICAN JOURNAL OF TRANSPLANTATION
Volume
23
Number
4
Start Page
565
End Page
572
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/102834
DOI
10.1016/j.ajt.2022.12.022
ISSN
1600-6135
Abstract
Diminished immune response to coronavirus disease 2019 (COVID-19) vaccines and breakthrough infection (BI) is a major concern for solid organ transplant recipients. Humoral and cellular immune responses of kidney transplant (KT) recipients after a third COVID-19 vaccination were investigated compared to matched health care workers. Anti-severe acute respiratory syndrome coronavirus 2 spike protein antibody and severe acute respi-ratory syndrome coronavirus 2 specific interferon-gamma releasing assay (IGRA) were assessed. A total of 38 KT recipients, including 20 BI and 18 noninfection, were evaluated. In the KT BI group, antibody titers were significantly increased (median 5 to 724, binding antibody units/mL (P = 0.002) after the third vaccination, but IGRA responses were negligible. After BI, antibody titers increased (median 11 355 binding antibody unit/mL; P < 0.001) and there was a significant increase of IGRA responses to spike proteins (Spike1-Nil, median 0.05 to 0.41 IU/mL; P = 0.009). Antibody titers and IGRA responses were significantly higher in the BI than in the non -infection group after 6 months. Immune responses were stronger in the health care worker than in the KT cohort, but the gap became narrower after BI. In conclusion, KT recipients who experienced BI after 3 COVID-19 vac-cinations acquired augmented humoral and cellular immune responses.
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