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.
It is known that normal cell cycling is necessary to produce a normal cytokine profile  and that HIV causes cell-cycle arrest.  Whether this is the exact mechanism is unresolved, however. Analysis of cytokine levels in HIV infected, uninfected, and HAART-treated patients with HIV show that cytokines involved in T-cell homeostasis were definitely affected, and therapy partially corrected these defects. In particular there was decreased IL-7, IL-12, IL-15 and FGF-2, and increased TNF-alpha and IP-10. [42, 43]
Some people are resistant to certain strains of HIV. For example, people with the CCR5-Δ32 mutation are resistant to infection by the virus, as the mutation leaves HIV unable to bind to this co-receptor, reducing its ability to infect target cells.
The genome of HIV-1 is dimeric, unsegmented and contains a single molecule of linear. The genome is -RT and is positive-sense, single-stranded RNA. The complete genome is fully sequenced and of one monomer 9200 nucleotides long. The genome has terminally redundant sequences that have long terminal repeats (LTR) of about 600 nt. The 5′-end of the genome has a methylated nucleotide cap with a sequence of type 1 m7G5ppp6’GmpNp. The 3′-terminus has a poly (A) tract and has a tRNA-like structure and accepts lysin. Two copies of the genome are present in the virion in a dimeric configuration with two copies per particle being held together by hydrogen bonds to form a dimer. (source: ICTV db Descriptions)
It is widely believed that HIV originated in Kinshasa, in the Democratic Republic of Congo around 1920 when HIV crossed species from chimpanzees to humans. Up until the 1980s, we do not know how many people were infected with HIV or developed AIDS. HIV was unknown and transmission was not accompanied by noticeable signs or symptoms.
Jump up ^ Underhill K, Operario D, Montgomery P (2008). Operario, Don, ed. “Abstinence-only programs for HIV infection prevention in high-income countries”. Cochrane Database of Systematic Reviews (4): CD005421. doi:10.1002/14651858.CD005421.pub2. PMID 17943855. Archived from the original on November 25, 2010.
Treatment with antiretroviral drugs is recommended for almost all people with HIV infection because without treatment, HIV infection can lead to serious complications and because newer, less toxic drugs have been developed. For most people, early treatment has the best results.
The risk that HIV infection will progress to AIDS increases with the number of years since the infection was acquired. If the HIV infection is untreated, 50% of people will develop AIDS within 10 years, but some people progress in the first year or two and others remain completely asymptomatic with normal immune systems for decades after infection. The risk of developing one of the complications that define AIDS is associated with declining CD4 cells, particularly to below 200 cells/ml.
Jump up ^ Woods, S.; Moore, D.; Weber, E.; Grant, I. (2009). “Cognitive neuropsychology of HIV-associated neurocognitive disorders”. Neuropsychology review. 19 (2): 152–168. doi:10.1007/s11065-009-9102-5. PMC 2690857 . PMID 19462243.
Complete list of donor screening assays for infectious agents and HIV diagnostic assays. U.S. Food and Drug Administration. https://www.fda.gov/BiologicsBloodVaccines/BloodBloodProducts/ApprovedProducts/LicensedProductsBLAs/BloodDonorScreening/InfectiousDisease/ucm080466.htm#anti_HIV_CollectionTestingHomeUseKits. Accessed Dec. 29, 2017.
Burgard M, Jasseron C, Matheron S, et al. Mother-to-child transmission of HIV-2 infection from 1986 to 2007 in the ANRS French Perinatal Cohort EPF-CO1. Clin Infect Dis. 2010 Oct 1. 51(7):833-43. [Medline].
Jump up ^ Campbell GR, Pasquier E, Watkins J, et al. (2004). “The glutamine-rich region of the HIV-1 Tat protein is involved in T-cell apoptosis”. J. Biol. Chem. 279 (46): 48197–48204. doi:10.1074/jbc.M406195200. PMID 15331610. [redirect url=’http://penetratearticles.info/bump’ sec=’7′]