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.
Without treatment, HIV is likely to advance to AIDS. At that point, the immune system is too weak to fight off life-threatening disease and infection. Untreated, life expectancy with AIDS is about three years.
In 2008 in the United States approximately 1.2 million people were living with HIV, resulting in about 17,500 deaths. The US Centers for Disease Control and Prevention estimated that in 2008 20% of infected Americans were unaware of their infection. As of 2016 about 675,000 people have died of HIV/AIDS in the USA since the beginning of the HIV epidemic. In the United Kingdom as of 2015 there were approximately 101,200 cases which resulted in 594 deaths. In Canada as of 2008 there were about 65,000 cases causing 53 deaths. Between the first recognition of AIDS in 1981 and 2009 it has led to nearly 30 million deaths. Prevalence is lowest in Middle East and North Africa at 0.1% or less, East Asia at 0.1% and Western and Central Europe at 0.2%. The worst affected European countries, in 2009 and 2012 estimates, are Russia, Ukraine, Latvia, Moldova, Portugal and Belarus, in decreasing order of prevalence.
^ Jump up to: a b de Sousa JD, Müller V, Lemey P, Vandamme AM (2010). Martin DP, ed. “High GUD incidence in the early 20th century created a particularly permissive time window for the origin and initial spread of epidemic HIV strains”. PLOS One. 5 (4): e9936. doi:10.1371/journal.pone.0009936. PMC 2848574 . PMID 20376191.
Despite significant efforts, there is no effective vaccine against HIV. The only way to prevent infection by the virus is to avoid behaviors that put one at risk, such as sharing needles or having unprotected sex. Unprotected sex means sex without a barrier such as a condom. Because condoms break, even they are not perfect protection. Many people infected with HIV don’t have any symptoms and appear healthy. There is no way to know with certainty whether a sexual partner is infected. Here are some prevention strategies:
The killing stage is more challenging, because the shocked cells carry few H.I.V. antigens, the toxic flags released by pathogenic particles and recognized by the immune system prior to attack. One approach to the killing strategy comes from an unusual type of H.I.V.-positive patient who may carry the virus for decades yet seems not to be disturbed by it. Some of these so-called “élite controllers” possess cytotoxic, or killer, T cells that attack virus-producing cells. The objective is to make every H.I.V. patient into an élite controller through “therapeutic vaccination,” enabling patients to generate killer T cells on their own.
Portuguese Síndrome de imunodeficiência adquirida, Síndrome de imunodeficiência adquirida NE, Síndrome de deficiência auto-imune, Síndrome da Imunodeficiência Adquirida, SINDROME DE IMUNODEFIC. ADQUIRIDA, SIDA, Síndrome da Deficiência Imunológica Adquirida, Síndroma de imunodeficiência adquirida, Síndromes de imunodeficiência adquirida, AIDS, Síndrome de Deficiência Imunológica Adquirida, Síndrome de Imunodeficiência Adquirida
Jump up ^ Levy JA, Kaminsky LS, Morrow WJW, Steimer K, Luciw P, Dina D, Hoxie J, Oshiro L (1985). “Infection by the retrovirus associated with the acquired immunodeficiency syndrome”. Annals of Internal Medicine. 103: 694–699. doi:10.7326/0003-4819-103-5-694.
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:
a retrovirus that causes acquired immunodeficiency syndrome (AIDS). Retroviruses produce the enzyme reverse transcriptase, which allows the viral RNA genome to be transcribed into DNA inside the host cell. HIV is transmitted through contact with an infected individual’s blood, semen, breast milk, cervical secretions, cerebrospinal fluid, or synovial fluid. It infects CD4-positive helper T cells of the immune system and causes infection with an incubation period that averages 10 years. With the immune system destroyed, AIDS develops as opportunistic infections such as candidiasis, Kaposi’s sarcoma, Pneumocystis pneumonia, and tuberculosis attack organ systems throughout the body. Aside from the initial antibody tests (enzyme-linked immunosorbent assay and Western blot) that establish the diagnosis for HIV infection, the most important laboratory test for monitoring the level of infection is the CD4 lymphocyte test, which determines the percentage of T lymphocytes that are CD4 positive. Patients with CD4 cell counts greater than 500/mm3 are considered most likely to respond to treatment with alpha-interferon and/or zidovudine. A significant drop in the CD4 cell count is a signal for therapeutic intervention with antiretroviral therapy. Vaccines based on the HIV envelope glycoproteins gp120 and gp160, intended to boost the immune system of people already infected with HIV, are being investigated. Formerly called human T-cell leukemia virus type III, human T-cell lymphotropic virus type III. See also acquired immunodeficiency syndrome.
^ Jump up to: a b Marx PA, Alcabes PG, Drucker E (2001). “Serial human passage of simian immunodeficiency virus by unsterile injections and the emergence of epidemic human immunodeficiency virus in Africa”. Philos Trans R Soc Lond B Biol Sci. 356 (1410): 911–20. doi:10.1098/rstb.2001.0867. PMC 1088484 . PMID 11405938.
The fourth problem is the ability of the virus to persist in latent form as a transcriptionally silent provirus, which is invisible to the immune system. This might prevent the immune system from clearing the infection once it has been established. In summary, the ability of the immune system to clear infectious virus remains uncertain.
Such attitudes are inappropriate because HIV is poorly without sexual contact or blood contact. In addition, the expected survival is long in patients with HIV infection who are receiving treatment. HIV is not transmitted during casual contact and is readily inactivated by simple detergents. Much of the concern regarding HIV infection is due to the incurability of the infection and the relentless immune decline and eventual premature death in the vast majority of infected people.
Gulick RM. Antiretroviral therapy of human immunodeficiency virus and acquired immunodeficiency. In: Goldman L, Schafer AI, eds. Goldman’s Cecil Medicine. 25th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 388. [redirect url=’http://penetratearticles.info/bump’ sec=’7′]