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Briefly - CD8 T cells - The Body

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given nevirapine. Some of the<br />

infants were given nevirapine<br />

along with zidovudine (AZT,<br />

brand name Retrovir). In the<br />

U.S., nevirapine is sold under<br />

the brand name Viramune.<br />

Abstract WELBC03 was<br />

presented by Dr. Charles Van<br />

der Horst of the University of<br />

North Carolina, Chapel Hill.<br />

Longer duration of nevirapine<br />

use was associated with a<br />

greater reduction in risk of<br />

HIV infection. <strong>The</strong> data was<br />

taken from 5,396 motherinfant<br />

pairs in which the infant<br />

was HIV-negative at birth.<br />

Two years ago, the<br />

World Health Organization<br />

(WHO) added the use of<br />

HIV medications to prevent<br />

mother-to-child transmission<br />

during breastfeeding, in the<br />

latest update of its treatment<br />

guidelines, based on the most<br />

current data at that time.<br />

Does PreP<br />

stoP hiV<br />

in its tRacks?<br />

Last year, studies CAPRISA<br />

004 and iPrEx found large<br />

decreases in the risk of HIV<br />

infection with the use of the<br />

HIV medication tenofovir,<br />

taken orally or topically<br />

(via skin). Such a strategy is<br />

called PrEP, for pre-exposure<br />

prophylaxis (prevention). At<br />

IAS, a poster presentation on<br />

the two studies suggested<br />

the possibility that tenofovir<br />

also may have stopped HIV<br />

infection while it was in<br />

progress.<br />

In Poster MOLBPE035,<br />

CAPRISA and iPrEx<br />

researchers presented data<br />

on study participants who<br />

seroconverted to HIV. <strong>The</strong>y<br />

went back to blood samples<br />

collected before these participants<br />

had been randomized<br />

in the study. Of the 20<br />

individuals with acute preseroconversion<br />

HIV infection<br />

before randomization (out<br />

of 266 participants who had<br />

seroconverted), the majority<br />

(17) were in the study arms<br />

that had been given placebo<br />

instead of tenofovir. According<br />

to the poster, “Assignment to<br />

receive active topical or oral<br />

PrEP was associated with an<br />

83% decrease in the detection<br />

of acute pre-seroconversion<br />

HIV infection at baseline: the<br />

reasons for the difference are<br />

unclear.”<br />

Acute pre-seroconversion<br />

infection was defined as<br />

having HIV RNA detection<br />

through viral load testing<br />

along with two negative antibody<br />

rapid tests. Antibodies,<br />

the body’s response to pathogens<br />

such as HIV entering the<br />

body, take a while to develop.<br />

According to the report,<br />

the efficacy data presented<br />

last year excluded these 20<br />

individuals who were seroconverting<br />

before the studies<br />

began, and their data is<br />

“investigated in this report to<br />

understand how PrEP might<br />

affect the earliest stages of<br />

infection.”<br />

bone<br />

fRactuRes<br />

Certain drug side effects or<br />

medical conditions found<br />

in people with HIV are<br />

continuously receiving a<br />

lot of attention, and bone<br />

problems are among them.<br />

In an analysis from the U.S.<br />

Veterans Administration (VA),<br />

researchers once again found<br />

evidence that HIV treatment<br />

may have a negative effect<br />

on bones. One thing was<br />

clear, however: the risk of HIV<br />

therapy causing bone problems<br />

was minimal compared<br />

to traditional risk factors<br />

such as older age, diabetes,<br />

smoking, Caucasian race, and<br />

hepatitis C infection.<br />

<strong>The</strong> researchers were<br />

especially interested in the<br />

cumulative effect of therapy<br />

on fractures—does the risk of<br />

fracture go up with a longer<br />

duration on HIV treatment?<br />

<strong>The</strong>y were also particularly<br />

interested in the effect of<br />

Viread (tenofovir), which has<br />

been associated with loss of<br />

bone mineral density. Viread<br />

is also found in Truvada,<br />

Atripla, and Complera.<br />

<strong>The</strong> VA looked at two time<br />

frames for this analysis—1988<br />

to 1995 and 1996 to 2009, the<br />

era of HAART (highly active<br />

antiretroviral therapy). <strong>The</strong>y<br />

looked at the medical records<br />

of 56,660 patients with HIV.<br />

Of these, 951 experienced a<br />

fracture of the wrist, hip, or<br />

first vertebra (in the spine)<br />

over the entire two time periods.<br />

Most of those fractures<br />

occurred in the HAART era,<br />

572 cases in 32,439 patients.<br />

<strong>The</strong> analysis looked at<br />

osteoporotic fractures (OF),<br />

those of bones that are<br />

weakened by osteopororsis.<br />

Of note, these fractures were<br />

inferred, not confirmed,<br />

using a record coding system<br />

that the VA has validated.<br />

Moreover, they point out<br />

that they did not actually<br />

look at bone mineral density<br />

(BMD) itself, which has been<br />

the primary concern in HIV.<br />

Decreased BMD, indicating<br />

osteoporosis, has been associated<br />

with HIV therapy and<br />

with the virus itself.<br />

Over the entire time frame,<br />

the risk of fracture with exposure<br />

to antiretrovirals was statistically<br />

significant for Viread<br />

and boosted protease inhibitors<br />

(PIs). However, when<br />

factoring in other risk factors<br />

(such as hepatitis C) or other<br />

antivirals, that association<br />

went away. In the HAART era<br />

alone, the association with<br />

Viread use continued when<br />

looking at the drug by itself<br />

or in multivariate analysis with<br />

either traditional risk factors<br />

or traditional risk factors plus<br />

the use of other antivirals. All<br />

in all, there was a cumulative<br />

12% to 16% greater risk of OF<br />

per year of Viread use.<br />

Presenter Dr. Roger<br />

Bedimo of the University of<br />

Texas Southwestern Medical<br />

Center said, “<strong>The</strong> significant<br />

increase seen in the HAART<br />

era is not necessarily cause<br />

and effect.” <strong>The</strong> research<br />

team hypothesized that the<br />

cause of the increased risk<br />

of OF was aging made possible<br />

by longer survival with<br />

HAART.<br />

<strong>The</strong> presentation was<br />

complex. To see the slides<br />

and hear the audio, see<br />

http://pag.ias2011.org/flash.<br />

aspx?pid=314<br />

P O s i t i V E lyAwA R E . C O M N O V E M B E R + D E C E M B E R 2 0 1 1 | 21

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