Anti-SARS CoV-2 IgG in COVID-19 Patients with Hematological Diseases: A Single-center, Retrospective Study in Japan

Objective Coronavirus disease (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread globally. Although the relationship between anti-SARS-CoV-2 immunoglobulin G (IgG) antibodies and COVID-19 severity has been reported, information is lacking regarding the ser...

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Published inInternal Medicine Vol. 61; no. 11; pp. 1681 - 1686
Main Authors Fujii, Takayuki, Hagihara, Masao, Mitamura, Keiko, Nakashima, Shiori, Ohara, Shin, Uchida, Tomoyuki, Inoue, Morihiro, Okuda, Moe, Yasuhara, Atsuhiro, Murakami, Jurika, Duong, Calvin, Iwatsuki-Horimoto, Kiyoko, Yamayoshi, Seiya, Kawaoka, Yoshihiro
Format Journal Article
LanguageEnglish
Published Japan The Japanese Society of Internal Medicine 01.06.2022
Japan Science and Technology Agency
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Summary:Objective Coronavirus disease (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread globally. Although the relationship between anti-SARS-CoV-2 immunoglobulin G (IgG) antibodies and COVID-19 severity has been reported, information is lacking regarding the seropositivity of patients with particular types of diseases, including hematological diseases. Methods In this single-center, retrospective study, we compared SARS-CoV-2 IgG positivity between patients with hematological diseases and those with non-hematological diseases. Results In total, 77 adult COVID-19 patients were enrolled. Of these, 30 had hematological disorders, and 47 had non-hematological disorders. The IgG antibody against the receptor-binding domain of the spike protein was detected less frequently in patients with hematological diseases (60.0%) than in those with non-hematological diseases (91.5%; p=0.029). Rituximab use was significantly associated with seronegativity (p=0.010). Conclusion Patients with hematological diseases are less likely to develop anti-SARS-CoV-2 antibodies than those with non-hematological diseases, which may explain the poor outcomes of COVID-19 patients in this high-risk group.
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Correspondence to Dr. Takayuki Fujii, supercjump@gmail.com
ISSN:0918-2918
1349-7235
1349-7235
DOI:10.2169/internalmedicine.9209-21