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Are We Forgetting About IgA? A Re-examination of Coronavirus Disease 2019 Convalescent Plasma.
Verkerke, Hans; Saeedi, Bejan J; Boyer, Darra; Allen, Jerry W; Owens, Joshua; Shin, Sooncheon; Horwath, Michael; Patel, Kashyap; Paul, Anu; Wu, Shang-Chuen; Wang, Jianmei; Ho, Alex; Maier, Cheryl L; Zerra, Patricia E; Chonat, Satheesh; Arthur, Connie M; Roback, John D; Neish, Andrew S; Lough, Christopher; Josephson, Cassandra D; Stowell, Sean R.
  • Verkerke H; Center for Transfusion Medicine and Cellular Therapies, Emory University, Atlanta, Georgia, USA.
  • Saeedi BJ; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Boyer D; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Allen JW; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Owens J; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Shin S; Center for Transfusion Medicine and Cellular Therapies, Emory University, Atlanta, Georgia, USA.
  • Horwath M; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Patel K; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Paul A; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Wu SC; Center for Transfusion Medicine and Cellular Therapies, Emory University, Atlanta, Georgia, USA.
  • Wang J; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Ho A; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Maier CL; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Zerra PE; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Chonat S; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Arthur CM; Center for Transfusion Medicine and Cellular Therapies, Emory University, Atlanta, Georgia, USA.
  • Roback JD; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Neish AS; Center for Transfusion Medicine and Cellular Therapies, Emory University, Atlanta, Georgia, USA.
  • Lough C; Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
  • Josephson CD; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Stowell SR; Center for Transfusion Medicine and Cellular Therapies, Emory University, Atlanta, Georgia, USA.
Transfusion ; 61(6): 1740-1748, 2021 06.
Article in English | MEDLINE | ID: covidwho-1243668
ABSTRACT

BACKGROUND:

While convalescent plasma (CP) may benefit patients with COVID-19, fundamental questions remain regarding its efficacy, including the components of CP that may contribute to its therapeutic effect. Most current serological evaluation of CP relies on examination of total immunoglobulin or IgG-specific anti-SARS-CoV-2 antibody levels. However, IgA antibodies, which also circulate and are secreted along the respiratory mucosa, represent a relatively uncharacterized component of CP. STUDY DESIGN AND

METHODS:

Residual samples from patients and CP donors were assessed for IgM, IgG, and IgA anti-SARS-CoV-2 antibody titers against the receptor-binding domain responsible for viral entry. Symptom onset was obtained by chart review.

RESULTS:

Increased IgA anti-SARS-CoV-2 antibody levels correlated with clinical improvement and viral clearance in an infant with COVID-19, prompting a broader examination of IgA levels among CP donors and hospitalized patients. Significant heterogeneity in IgA levels was observed among CP donors, which correlated weakly with IgG levels or the results of a commonly employed serological test. Unlike IgG and IgM, IgA levels were also more likely to be variable in hospitalized patients and this variability persisted in some patients >14 days following symptom onset. IgA levels were also less likely to be sustained than IgG levels following subsequent CP donation.

CONCLUSIONS:

IgA levels can be very heterogenous among CP donors and hospitalized patients and do not necessarily correlate with commonly employed testing platforms. Examining isotype levels in CP and COVID-19 patients may allow for a tailored approach when seeking to fill specific gaps in humoral immunity.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin A / Convalescence / SARS-CoV-2 / COVID-19 Type of study: Case report / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Female / Humans / Infant Country/Region as subject: North America Language: English Journal: Transfusion Year: 2021 Document Type: Article Affiliation country: Trf.16435

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin A / Convalescence / SARS-CoV-2 / COVID-19 Type of study: Case report / Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Female / Humans / Infant Country/Region as subject: North America Language: English Journal: Transfusion Year: 2021 Document Type: Article Affiliation country: Trf.16435