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Prior Infection and Passive Transfer of Neutralizing Antibody Prevent Replication of Severe Acute Respiratory Syndrome Coronavirus in the Respiratory Tract of Mice

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Journal J Virol
Date 2004 Mar 16
PMID 15016880
Citations 284
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Abstract

Following intranasal administration, the severe acute respiratory syndrome (SARS) coronavirus replicated to high titers in the respiratory tracts of BALB/c mice. Peak replication was seen in the absence of disease on day 1 or 2, depending on the dose administered, and the virus was cleared within a week. Viral antigen and nucleic acid were detected in bronchiolar epithelial cells during peak viral replication. Mice developed a neutralizing antibody response and were protected from reinfection 28 days following primary infection. Passive transfer of immune serum to naïve mice prevented virus replication in the lower respiratory tract following intranasal challenge. Thus, antibodies, acting alone, can prevent replication of the SARS coronavirus in the lung, a promising observation for the development of vaccines, immunotherapy, and immunoprophylaxis regimens.

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References
1.
Renegar K . Influenza virus infections and immunity: a review of human and animal models. Lab Anim Sci. 1992; 42(3):222-32. View

2.
Vennema H, de Groot R, Harbour D, Dalderup M, Gruffydd-Jones T, Horzinek M . Early death after feline infectious peritonitis virus challenge due to recombinant vaccinia virus immunization. J Virol. 1990; 64(3):1407-9. PMC: 249267. DOI: 10.1128/JVI.64.3.1407-1409.1990. View

3.
Olsen C . A review of feline infectious peritonitis virus: molecular biology, immunopathogenesis, clinical aspects, and vaccination. Vet Microbiol. 1993; 36(1-2):1-37. PMC: 7117146. DOI: 10.1016/0378-1135(93)90126-r. View

4.
Crowe Jr J, Bui P, London W, Davis A, HUNG P, Chanock R . Satisfactorily attenuated and protective mutants derived from a partially attenuated cold-passaged respiratory syncytial virus mutant by introduction of additional attenuating mutations during chemical mutagenesis. Vaccine. 1994; 12(8):691-9. DOI: 10.1016/0264-410x(94)90218-6. View

5.
Epstein S, Lo C, Misplon J, Lawson C, Hendrickson B, Max E . Mechanisms of heterosubtypic immunity to lethal influenza A virus infection in fully immunocompetent, T cell-depleted, beta2-microglobulin-deficient, and J chain-deficient mice. J Immunol. 1997; 158(3):1222-30. View