Antibody titers against SARS-CoV-2 decline, but do not disappear for several months

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. Sequential blood samples were collec...

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Published inEClinicalMedicine Vol. 32; p. 100734
Main Authors 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
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.02.2021
Elsevier
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Abstract 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. 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. 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. 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. The Japan Agency for Medical Research and Development and the National Institutes of Allergy and Infectious Diseases.
AbstractList 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.BACKGROUNDTo 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.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.METHODSSequential 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.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.FINDINGSThe 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.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.INTERPRETATIONAlthough 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.The Japan Agency for Medical Research and Development and the National Institutes of Allergy and Infectious Diseases.FUNDINGThe Japan Agency for Medical Research and Development and the National Institutes of Allergy and Infectious Diseases.
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.
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. 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. 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. 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. The Japan Agency for Medical Research and Development and the National Institutes of Allergy and Infectious Diseases.
AbstractBackgroundTo 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. MethodsSequential 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. FindingsThe 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. InterpretationAlthough 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. FundingThe Japan Agency for Medical Research and Development and the National Institutes of Allergy and Infectious Diseases.
ArticleNumber 100734
Author Koga, Michiko
Mitamura, Keiko
Suzuki, Tetsuya
Yotsuyanagi, Hiroshi
Adachi, Eisuke
Nakachi, Ichiro
Baba, Rie
Saito, Makoto
Yamayoshi, Seiya
Maeda, Kenji
Omagari, Norio
Yagi, Kazuma
Hattori, Shin-ichiro
Miyazato, Yusuke
Yamamoto, Shinya
Murakami, Jurika
Sugaya, Norio
Okuda, Moe
Yasuhara, Atsuhiro
Iwatsuki-Horimoto, Kiyoko
Fujita, Kensuke
Akasaka, Osamu
Kato, Hideaki
Hamabata, Taiki
Mitsuya, Hiroaki
Nagai, Hiroyuki
Nakajima, Hideaki
Nakamura, Morio
Ochi, Junichi
Kawaoka, Yoshihiro
Ogura, Takayuki
Pattinson, David
Ito, Mutsumi
Nojima, Masanori
Chiba, Shiho
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  surname: Yamayoshi
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  organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan
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  givenname: Atsuhiro
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  organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan
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  givenname: Mutsumi
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  organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan
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  organization: Emergency Medical Center, Fujisawa City Hospital, Japan
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  organization: Department of Pulmonary Medicine, Tokyo Saiseikai Central Hospital, Japan
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  organization: Pulmonary division, Department of Internal Medicine, Saiseikai Utsunomiya Hospital, Japan
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  givenname: Michiko
  surname: Koga
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  organization: Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Japan
– sequence: 8
  givenname: Keiko
  surname: Mitamura
  fullname: Mitamura, Keiko
  organization: Division of Infection Control, Eiju General Hospital, Japan
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  givenname: Kazuma
  surname: Yagi
  fullname: Yagi, Kazuma
  organization: Department of Pulmonary Medicine, Department of Medicine, Keiyu Hospital, Japan
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  surname: Maeda
  fullname: Maeda, Kenji
  organization: Department of Refractory Viral Infections, National Center for Global Health and Medicine Research Institute, Japan
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  givenname: Hideaki
  surname: Kato
  fullname: Kato, Hideaki
  organization: Infection Prevention and Control Department, Yokohama City University Hospital, Japan
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  fullname: Nojima, Masanori
  organization: Center for Translational Research, Institute of Medical Science Hospital, University of Tokyo, Japan
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  surname: Pattinson
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  organization: Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, USA
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  surname: Ogura
  fullname: Ogura, Takayuki
  organization: Department of Emergency Medicine and Critical Care Medicine, Saiseikai Utsunomiya Hospital, Japan
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  givenname: Rie
  surname: Baba
  fullname: Baba, Rie
  organization: Pulmonary division, Department of Internal Medicine, Saiseikai Utsunomiya Hospital, Japan
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  givenname: Kensuke
  surname: Fujita
  fullname: Fujita, Kensuke
  organization: Department of Emergency Medicine and Critical Care Medicine, Saiseikai Utsunomiya Hospital, Japan
– sequence: 17
  givenname: Hiroyuki
  surname: Nagai
  fullname: Nagai, Hiroyuki
  organization: Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of Institute of Medical Science, the University of Tokyo, Japan
– sequence: 18
  givenname: Shinya
  surname: Yamamoto
  fullname: Yamamoto, Shinya
  organization: Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Japan
– sequence: 19
  givenname: Makoto
  surname: Saito
  fullname: Saito, Makoto
  organization: Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Japan
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  givenname: Eisuke
  surname: Adachi
  fullname: Adachi, Eisuke
  organization: Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of Institute of Medical Science, the University of Tokyo, Japan
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  surname: Ochi
  fullname: Ochi, Junichi
  organization: Department of Respiratory Medicine, Eiju General Hospital, Japan
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  organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan
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  email: yoshihiro.kawaoka@wisc.edu
  organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Japan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33589882$$D View this record in MEDLINE/PubMed
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Snippet To develop an effective vaccine against a novel viral pathogen, it is important to understand the longitudinal antibody responses against its first infection....
AbstractBackgroundTo develop an effective vaccine against a novel viral pathogen, it is important to understand the longitudinal antibody responses against its...
Background: To develop an effective vaccine against a novel viral pathogen, it is important to understand the longitudinal antibody responses against its first...
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SubjectTerms Internal Medicine
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Title Antibody titers against SARS-CoV-2 decline, but do not disappear for several months
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