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HIV-Mycobacterium tuberculosis co-infection: a `danger-couplemodel of disease pathogenesis

Shankar, Esaki M. (author)
University of Malaya, Malaysia
Vignesh, Ramachandran (author)
YRG Centre AIDS Research and Educ YRG CARE, India
Ellegård, Rada (author)
Linköpings universitet,Avdelningen för mikrobiologi och molekylär medicin,Hälsouniversitetet
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Barathan, Muttiah (author)
University of Malaya, Malaysia
Chong, Yee K. (author)
University of Malaya, Malaysia
Bador, M. Kahar (author)
University of Malaya, Malaysia
Rukumani, Devi V. (author)
University of Malaya, Malaysia
Sabet, Negar S. (author)
SEGi University, Malaysia
Kamarulzaman, Adeeba (author)
University of Malaya, Malaysia
Velu, Vijayakumar (author)
Emory Vaccine Centre, GA USA
Larsson, Marie (author)
Linköpings universitet,Avdelningen för mikrobiologi och molekylär medicin,Hälsouniversitetet
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 (creator_code:org_t)
Wiley / Blackwell Publishing Ltd, 2014
2014
English.
In: PATHOGENS AND DISEASE. - : Wiley / Blackwell Publishing Ltd. - 2049-632X. ; 70:2, s. 110-118
  • Research review (peer-reviewed)
Abstract Subject headings
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  • Tuberculosis (TB) and human immunodeficiency virus (HIV) infection interfere and impact the pathogenesis phenomena of each other. Owing to atypical clinical presentations and diagnostic complications, HIV/TB co-infection continues to be a menace for healthcare providers. Although the increased access to highly active antiretroviral therapy (HAART) has led to a reduction in HIV-associated opportunistic infections and mortality, the concurrent management of HIV/TB co-infection remains a challenge owing to adverse effects, complex drug interactions, overlapping toxicities and tuberculosis -associated immune reconstitution inflammatory syndrome. Several hypotheses have been put forward for the exacerbation of tuberculosis by HIV and vice versa supported by immunological studies. Discussion on the mechanisms produced by infectious cofactors with impact on disease pathology could shed light on how to design potential interventions that could decelerate disease progression. With no vaccine for HIV and lack of an effective vaccine for tuberculosis, it is essential to design strategies against HIV–TB co-infection.

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