Interaction of Influenza Virus with Blood Platelets

Author:

TERADA HIDEO12,BALDINI MARIO13,EBBE SHIRLEY14,MADOFF MORTON A.15

Affiliation:

1. Blood Research Laboratory and the Infectious Disease Laboratory, New England Center Hospitals and Tufts University School of Medicine, Boston, Mass.

2. Blood Research Laboratory, New England Medical Center Hospitals. Present address: Showa University Medical School, Tokyo, Japan.

3. Blood Research Laboratory, New England Medical Center Hospitals; Associate Professor of Medicine, Tufts University School of Medicine. Present address: Division of Hematologic Research, Brown University, Institute for Health Sciences and Memorial Hospital, Pawtucket, R. I.

4. Blood Research Laboratory, New England Medical Center Hospitals; Assistant Professor of Medicine, Tufts University School of Medicine. Present address: St. Elizabeth's Hospital, Brighton, Mass.

5. New England Medical Center Hospitals, Assistant Professor of Medicine, Tufts University School of Medicine. Present address: Lemuel Shattuck Hospital, Boston, Mass.

Abstract

Abstract The interaction of human blood platelets with influenza virus (PR-8) was studied in vitro and in vivo. It was found that "live" influenza virus was rapidly adsorbed onto human blood platelets at 4 C. and completely eluted at 37 C. "Dead" virus was adsorbed at 4 C. but not eluted at 37 C. unless the platelets were treated with RDE (receptor destroying enzyme). Adorption of virus also occurred at tem peratures above 4 C. (from 20 to 37 C.). However, while adsorption was maintained throughout incubation at 4 C., slow elution occurred after 30 to 90 minutes incubation at 26 to 37 C. Storage of the platelets for lengthy intervals at 4 C. or coating of the platelets with macromolecules did not interfere with virus adsorption. After one cycle of adsorption-elution, blood platelets could not adsorb virus again. Treatment with RDE greatly reduced virus adsorption. During the process of virus adsorption, prominent platelet clumping occurred. During elution, clumping remained unchanged, and gross alterations in morphology of the platelets were observed. In the process of virus adsorption-elution, large numbers of platelets were lysed. Comparative experiments were performed simultaneously with human red blood cells (RBC) and identical results were obtained as with blood platelets. However, the extent of adsorption of live virus was equal for platelets and RBC only when the relationship between platelet number and RBC number in the preparations used was 6:1. This suggested a direct proportion between the surface area of both platelet and RBC and the number of available virus receptors. Virus suspensions infused into rabbits produced a sharp and sustained drop of the platelet count. Survival of radioactively labeled platelets treated with virus prior to infusion was markedly shortened with live virus and was only slightly reduced with dead virus. It is suggested from these experiments that blood platelets, as other blood cells, may serve as carriers of viruses in the circulation and that in this process the platelets are damaged and partially destroyed.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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