Risk factors
Drug hypersensitivity reactions do not occur in everyone who uses a given drug, and a variety of factors may increase the risk. In general, women are more susceptible, as are older individuals[1]. People with more intact immune systems seem more prone to certain types of immune-mediated hypersensitivity. However, the rate of hypersensitivity is higher in people with HIV[2]. Individuals who have experienced drug-induced hypersensitivity reactions in the past are more likely to do so again, as are people with a history of allergic conditions such as asthma.
For abacavir (Ziagen) hypersensitivity, risk factors seen in various studies include male sex, African ethnicity, more advanced HIV disease and history of allergies[3]. In one 50-person study, 18% of individuals with primary HIV infection developed a hypersensitivity reaction[4].
Nevirapine (Viramune) hypersensitivity is more common in women and people with higher CD4 cell counts. Other risk factors include low body weight, co-infection with hepatitis B or C and certain genetic patterns[5][6].
Several types of hypersensitivity appear linked to genetic predisposition[7]. Most patients with abacavir hypersensitivity carry the HLA-B*5701 haplotype[8][9]. This genetic pattern may be present in as many as 10% of the population, and is more common amongst Caucasians than people of African descent. For more information, see Abacavir hypersensitivity reaction.
latest aidsmap news
- High rate of death amongst patients with HIV diagnosed late
- CD4 cell count increases sustained up to five years in developing-world treatment programmes
- Raltegravir may have role in PEP if exposure involves drug-resistant HIV
- Excellent outcomes from five years of antiretroviral use in Botswana
- Study explores verbal and non-verbal communication in unprotected sex between men
- IL-2 provides quick ‘AIDS rescue’, but effect does not always last
- Once-a-day etravirine should work as first-line treatment
- Second-line combinations fail twice as often as first-line ones in the first year
- If you can't switch, better to stay on failing treatment than stop it, studies show
- Non-nucleoside resistance is efficiently transmitted within infection ‘clusters’
