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Infection and Immunity, November 2001, p. 6676-6682, Vol. 69, No. 11
Department of Respiratory Medicine, National
Heart and Lung Institute,1 and
Departments of Pathology3 and
Infectious Diseases and Microbiology,2
Imperial College School of Medicine, London, United Kingdom
Received 2 April 2001/Returned for modification 24 May
2001/Accepted 26 July 2001
With a view to exploring the role of transforming growth factor
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.11.6676-6682.2001
Enhanced Antimycobacterial Response to Recombinant
Mycobacterium bovis BCG Expressing
Latency-Associated Peptide
(TGF-
) during mycobacterial infection, recombinant clones of
bacillus Calmette-Guérin (BCG) were engineered to express the
natural antagonist of TGF-
, latency-activated peptide (LAP). Induction of TGF-
activity was reduced when macrophages were infected with BCG expressing the LAP construct (LAP-BCG). There was a
significant reduction in the growth of LAP-BCG in comparison to that of
control BCG following intravenous infection in a mouse model. The
enhanced control of mycobacterial replication was associated with an
increase in the production of gamma interferon by splenocytes challenged during the acute stage of infection but with a diminished recall response assessed after 13 weeks. Organ weight and
hydroxyproline content, representing tissue pathology, were also lower
in mice infected with LAP-BCG. The results are consistent with the
hypothesis that TGF-
has a detrimental effect on mycobacterial
immunity. While a reduction in TGF-
activity augments the initial
response to BCG vaccination, early bacterial clearance may adversely
affect the induction of a long-term memory response by LAP-BCG.
*
Corresponding author. Mailing address: Department of
Respiratory Medicine, Southampton University Hospitals NHS Trust,
Southampton, Hampshire, United Kingdom. Phone: 44 2380 796228. Fax: 44 2380 794585. E-mail:ben.marshall{at}suht.swest.nhs.uk.
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