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Worldwide, half of all individuals infected with HIV are also
infected with TB.
Tuberculosis (TB) and AIDS, the most important
infectious causes of death in the world, share many
similarities and contrasts in demography, transmission
and pathogenesis.
The huge research interest in
HIV has meant that more is known about this virus,
its dynamics and pathogenesis than any other.
Incontrast, although TB has been a scourge to
humanity for thousands of years, much less is known
about the basic pathogenetic mechanisms which
cause the disease.
One-third of all HIV deaths are attributable to
TB, and the lifetime risk of an HIV positive person developing
TB is 50% compared with 5–10% for an uninfected individual.
In an individual previously infected with TB (Mantoux positive),
the lifetime risk of reactivation is 5–7%, in contrast to an
annual 10% risk in patients co-infected with HIV.
The main reason for the strong association between the two
diseases has been considered to be the high rate of
reactivation.
However, since TB and HIV flourish in
similar poor socio-economic circumstances, it is likely
that another important cause is recent infection, with
the development of active disease as a result of
immunosuppression.
In Africa, TB tends to occur in
HIV infected individuals with high CD4 counts, and is
likely to be a reflection of progressive primary disease.
In contrast, in the USA, the median CD4 count at
presentation with TB is low (<200 cells/mm3) and even
lower for disseminated disease (<100 cells/mm3), probably
reflecting the reactivation of quiescent primary
infection in severely immunosuppressed patients.
TB in an HIV positive individual is associated with
falls in the CD4 count and rises in the viral load. These
changes are not specific to TB – any infection causing
activation of HIV via cellular mechanisms, including
Nkb and changes in the cytokine milieu which favour
HIV replication, will produce similar effects. There is
no epidemiological evidence that TB worsens the prognosis
of HIV.
Similarly, TB prevention in the
form of chemoprophylaxis may not improve the overall
mortality of HIV. Nevertheless, control measures
directed against TB would have a marked benefit on the
health of the HIV population worldwide.
This article is
based on the
Mitchell Lecture,
given at Ipswich on
6 March 2000 by
Brian Gazzard
Consultant
Physician and
Research Director,
HIV/GUM, Chelsea
and Westminster
Hospital, London
Key Points
***The HIV epidemic has been associated with an enormous
increase in the pandemic of tuberculosis (TB)
***In a minority of patients with HIV, a particular genetic
constitution allows long-term control of infection. This is
likely to be true of TB
***Mycobacterium tuberculosis is an organism that grows in
macrophages. The induced cellular and cytokine responses
are responsible not only for disease control or progression
but also for the pathogenesis of the infection
***Successful treatment of HIV and TB infection requires long
term adherence to multi drug regimens in order to avoid
drug resistance
Clin Med JRCPL 2001 1.62-8
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