High viral load main risk factor in mother-to-baby transmission

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Combination therapy which can suppress viral load

below the limit of detection (less than 500 copies) is likely to be advocated

even more strongly to pregnant HIV-positive women following the publication of

Glossary

detectable viral load

When viral load is detectable, this indicates that HIV is replicating in the body. If the person is taking HIV treatment but their viral load is detectable, the treatment is not working properly. There may still be a risk of HIV transmission to sexual partners.

perinatal

Relating to the period around the time of birth. Perinatal transmission is when HIV is passed on during pregnancy, childbirth or breastfeeding. People with perinatally-acquired HIV have been living with HIV since birth or infancy.

monotherapy

Taking a drug on its own, rather than in combination with other drugs.

perinatal

Relating to the period starting a few weeks before birth and including the birth and a few weeks after birth.

protocol

A detailed research plan that describes the aims and objectives of a clinical trial and how it will be conducted.

two studies which showed that not one woman with undetectable viral load passed

on HIV to her child. In comparison, one of the studies found that 63% of

untreated women with viral load above 100,000 copies gave birth to HIV-positive

babies.

Writing in the New England Journal of Medicine last

week, Patricia Garcia of Prentice Women's Hospital, Chicago, reported results

from the Women and Infants Transmission Study. This study measured viral load

and HIV transmission in 552 women offered AZT monotherapy during pregnancy

according to the ACTG 076 protocol (LINK to record).

In the same edition, Lynn Mofenson of the US National

Institute of Child Health and Development reported on the relationship between

viral load and transmission in PACTG 185, a study which investigated whether it

was beneficial to add hyperimmune globulin to AZT monotherapy during pregnancy

(no difference in transmission rates was found). Mofenson reported that none of

the mothers with undetectable viral load at the time of delivery transmitted HIV

to their infants.

On average, women who did not transmit HIV to their

infants had viral load in the region of 3,000 -4,000 copies, compared to an

average of 30,000 - 40,000 copies amongst women who did transmit HIV to their

infants. However, there was a significant difference in risk of transmission

between mothers with viral load below 500 copies and mothers with a low but

detectable viral load of less than 5,000 copies.

The Women and Infant Transmission Study found

substantial levels of HIV transmission even amongst women who would be

considered to have low viral load according to current HIV treatment

guidelines:

Mean viral load during pregnancy

Transmission rate on treatment

Transmission rate without treatment

0%

0%

1,000 - 10,000

12%

20%

10,000 - 50,000

17.3%

24%

50,000 - 100,000

31 %

31%

>100,000

20%

63%

Reducing viral load to a low but detectable level did not always prevent HIV

transmission in those who received AZT during pregnancy. However, the study was

not able to distinguish whether other factors (such as mode of delivery, time

from rupture of membranes to birth, low birth weight, illicit drug use, smoking

or trial site) were associated with an increased risk of transmission in the

group with low but detectable viral load on treatment.

 Other findings

  • Women who received zidovudine (AZT) were less likely to pass on HIV to their

    babies (note that both studies were carried out before the widespread

    introduction of HAART)

  • No significant difference was found in viral load levels between mothers who

    transmitted early in pregnancy and those who transmitted later on, or during

    delivery. 72% of HIV-positive infants were believed to have been infected late

    in pregnancy or during delivery in the Women and Infants Transmission

    Study.

References

Garcia P et al. Maternal levels of plasma human immunodeficiency virus type 1

RNA and the risk of perinatal transmission. NEJM 341: 394-402, 1999.

Mofenson L et al. Risk factors for perinatal transmission of human

immunodeficiency virus type 1 in women treated with zidovudine. NEJM 341:

385-93, 1999.