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Antibody titers against SARS-CoV-2 decline, but do not disappear for several months.
Yamayoshi, Seiya; Yasuhara, Atsuhiro; Ito, Mutsumi; Akasaka, Osamu; Nakamura, Morio; Nakachi, Ichiro; Koga, Michiko; Mitamura, Keiko; Yagi, Kazuma; Maeda, Kenji; Kato, Hideaki; Nojima, Masanori; Pattinson, David; Ogura, Takayuki; Baba, Rie; Fujita, Kensuke; Nagai, Hiroyuki; Yamamoto, Shinya; Saito, Makoto; Adachi, Eisuke; Ochi, Junichi; Hattori, Shin-Ichiro; Suzuki, Tetsuya; Miyazato, Yusuke; Chiba, Shiho; Okuda, Moe; Murakami, Jurika; Hamabata, Taiki; Iwatsuki-Horimoto, Kiyoko; Nakajima, Hideaki; Mitsuya, Hiroaki; Omagari, Norio; Sugaya, Norio; Yotsuyanagi, Hiroshi; Kawaoka, Yoshihiro.
  • Yamayoshi S; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan.
  • Yasuhara A; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan.
  • Ito M; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan.
  • Akasaka O; Emergency Medical Center, Fujisawa City Hospital, Japan.
  • Nakamura M; Department of Pulmonary Medicine, Tokyo Saiseikai Central Hospital, Japan.
  • Nakachi I; Pulmonary division, Department of Internal Medicine, Saiseikai Utsunomiya Hospital, Japan.
  • Koga M; Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Japan.
  • Mitamura K; Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of Institute of Medical Science, the University of Tokyo, Japan.
  • Yagi K; Division of Infection Control, Eiju General Hospital, Japan.
  • Maeda K; Department of Pulmonary Medicine, Department of Medicine, Keiyu Hospital, Japan.
  • Kato H; Department of Refractory Viral Infections, National Center for Global Health and Medicine Research Institute, Japan.
  • Nojima M; Infection Prevention and Control Department, Yokohama City University Hospital, Japan.
  • Pattinson D; Department of Hematology and Clinical Immunology, Yokohama City University School of Medicine, Japan.
  • Ogura T; Center for Translational Research, Institute of Medical Science Hospital, University of Tokyo, Japan.
  • Baba R; Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, USA.
  • Fujita K; Department of Emergency Medicine and Critical Care Medicine, Saiseikai Utsunomiya Hospital, Japan.
  • Nagai H; Pulmonary division, Department of Internal Medicine, Saiseikai Utsunomiya Hospital, Japan.
  • Yamamoto S; Department of Emergency Medicine and Critical Care Medicine, Saiseikai Utsunomiya Hospital, Japan.
  • Saito M; Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of Institute of Medical Science, the University of Tokyo, Japan.
  • Adachi E; Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Japan.
  • Ochi J; Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of Institute of Medical Science, the University of Tokyo, Japan.
  • Hattori SI; Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Japan.
  • Suzuki T; Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of Institute of Medical Science, the University of Tokyo, Japan.
  • Miyazato Y; Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of Institute of Medical Science, the University of Tokyo, Japan.
  • Chiba S; Department of Respiratory Medicine, Eiju General Hospital, Japan.
  • Okuda M; Department of Refractory Viral Infections, National Center for Global Health and Medicine Research Institute, Japan.
  • Murakami J; Disease Control and Prevention Center, National Center for Global Health and Medicine Hospital, Japan.
  • Hamabata T; Disease Control and Prevention Center, National Center for Global Health and Medicine Hospital, Japan.
  • Iwatsuki-Horimoto K; Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, USA.
  • Nakajima H; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan.
  • Mitsuya H; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan.
  • Omagari N; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan.
  • Sugaya N; Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan.
  • Yotsuyanagi H; Department of Hematology and Clinical Immunology, Yokohama City University School of Medicine, Japan.
  • Kawaoka Y; Department of Refractory Viral Infections, National Center for Global Health and Medicine Research Institute, Japan.
EClinicalMedicine ; 32: 100734, 2021 Feb.
Article in English | MEDLINE | ID: covidwho-1385450
ABSTRACT

BACKGROUND:

To develop an effective vaccine against a novel viral pathogen, it is important to understand the longitudinal antibody responses against its first infection. Here we performed a longitudinal study of antibody responses against SARS-CoV-2 in symptomatic patients.

METHODS:

Sequential blood samples were collected from 39 individuals at various timepoints between 0 and 154 days after onset. IgG or IgM titers to the receptor binding domain (RBD) of the S protein, the ectodomain of the S protein, and the N protein were determined by using an ELISA. Neutralizing antibody titers were measured by using a plaque reduction assay.

FINDINGS:

The IgG titers to the RBD of the S protein, the ectodomain of the S protein, and the N protein peaked at about 20 days after onset, gradually decreased thereafter, and were maintained for several months after onset. Extrapolation modeling analysis suggested that the IgG antibodies were maintained for this amount of time because the rate of reduction slowed after 30 days post-onset. IgM titers to the RBD decreased rapidly and disappeared in some individuals after 90 days post-onset. All patients, except one, possessed neutralizing antibodies against authentic SARS-CoV-2, which they retained at 90 days after onset. The highest antibody titers in patients with severe infections were higher than those in patients with mild or moderate infections, but the decrease in antibody titer in the severe infection cohort was more remarkable than that in the mild or moderate infection cohort.

INTERPRETATION:

Although the number of patients is limited, our results show that the antibody response against the first SARS-CoV-2 infection in symptomatic patients is typical of that observed in an acute viral infection.

FUNDING:

The Japan Agency for Medical Research and Development and the National Institutes of Allergy and Infectious Diseases.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Journal: EClinicalMedicine Year: 2021 Document Type: Article Affiliation country: J.ECLINM.2021.100734

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Language: English Journal: EClinicalMedicine Year: 2021 Document Type: Article Affiliation country: J.ECLINM.2021.100734