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Cited by 903

The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.

The convalescent sera option for containing COVID-19

Open access
Casadevall, Arturo, Pirofski, Liise-anne·2020·Journal of Clinical Investigation

Abstract

As of early 2020, humanity is confronting a pandemic in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).SARS-CoV-2 causes coronavirus disease, abbreviated as COVID-19.At the time of this writing, SARS-CoV-2 is spreading in multiple countries, threatening a pandemic that will affect billions of people.This virus appears to be a new human pathogen.Currently there are no vaccines, monoclonal antibodies (mAbs), or drugs available for SARS-CoV-2, although many are in rapid development and some may be available in a short time.This Viewpoint argues that human convalescent serum is an option for prevention and treatment of COVID-19 disease that could be rapidly available when there are sufficient numbers of people who have recovered and can donate immunoglobulin-containing serum.

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Registry

Crossref · 10.1172/jci138003

Cites

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Cites

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Metadata

Authors
Casadevall, A., & Pirofski, L.-A.
Venue
Journal of Clinical Investigation
Published
2020-03-13
Volume
130
Issue
4
Pages
1545-1548
ISSN
  • 0021-9738 (ISSN-L)
  • 1558-8238
OpenAlex
W3011379523
Cited by
903
References
27
FWCI
25.71
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: The convalescent sera option for containing COVID-19. https://app.cochat.ai/papers/10.1172/jci138003
The paper
Casadevall, A., & Pirofski, L.-A. (2020). The convalescent sera option for containing COVID-19. Journal of Clinical Investigation. https://doi.org/10.1172/jci138003

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.