Type C retrovirus inactivation by human complement is determined by both the viral genome and the producer cell.

Abstract:

:The inactivation of type C retroviruses by human serum may be a considerable impediment to the use of retroviral vectors in vivo for gene therapy. Here we show that virus inactivation is dependent both on the virus and on the cell line used to produce the virus. All viruses produced from murine NIH 3T3 or dog Cf2ThS+L- cells are sensitive to human serum. In contrast, those produced from mink Mv-1-Lu and human HOS or TE671 cells are at least partially resistant, with the exception of murine leukemia viruses. In particular, the feline endogenous virus RD114 is completely resistant to a panel of eight human sera when produced from Mv-1-Lu or HOS cells. This differential resistance is controlled by the viral envelope proteins. Virus inactivation can be correlated with the ability of the producer cells to be lysed by human serum. Inactivation of sensitive viruses requires the classical pathway of complement but does not require virion lysis.

journal_name

J Virol

journal_title

Journal of virology

authors

Takeuchi Y,Cosset FL,Lachmann PJ,Okada H,Weiss RA,Collins MK

doi

10.1128/JVI.68.12.8001-8007.1994

subject

Has Abstract

pub_date

1994-12-01 00:00:00

pages

8001-7

issue

12

eissn

0022-538X

issn

1098-5514

journal_volume

68

pub_type

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