MURAMYL DIPEPTIDE INHIBITS REPLICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS INVITRO

被引:11
|
作者
MASIHI, KN
LANGE, W
ROHDESCHULZ, B
CHEDID, L
机构
[1] UNIV S FLORIDA,H LEE MOFFITT CANC CTR,TAMPA,FL 33682
[2] UNIV S FLORIDA,RES INST,TAMPA,FL 33682
关键词
D O I
10.1089/aid.1990.6.393
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the search for compounds capable of inducing endogenous production of colony-stimulating factor (CSF) and possessing activity against human immunodeficiency virus (HIV), an immunomodulator, muramyl dipeptide (MDP), was investigated. MDP can enhance monocyte-macrophage CSF in serum and promote nonspecific resistance against a variety of microbial pathogens. MDP exhibited an inhibitory activity against HIV infection of CD4+ H9 lymphocytes and U937 monocytoid cells. An inhibitor of viral reverse transcriptase, 2′, 3′-dideoxyadenosine, produced potent inhibition in cultures which were similarly infected with HIV. MDP could partially reduce antigen production in persistently HIV-infected KE37/1 lymphocyte cultures. © 1990, Mary Ann Liebert, Inc. All rights reserved.
引用
收藏
页码:393 / 399
页数:7
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