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If the CD4 count is low, people are more likely to develop serious infections and other complications of HIV such as certain cancers. Viral load helps predict how fast the CD4 count is likely to decrease over the next few years.

Jump up ^ Surveillance; riques, Risk Assessment Division = Le VIH et le sida au Canada: rapport de surveillance en date du 31 décembre 2009 / Division de la surveillance et de l’évaluation des (2010). HIV and AIDS in Canada : surveillance report to December 31, 2009 (PDF). Ottawa: Public Health Agency of Canada, Centre for Communicable Diseases and Infection Control, Surveillance and Risk Assessment Division. ISBN 978-1-100-52141-1. Archived from the original (PDF) on January 19, 2012.

These subtypes are sometimes further split into sub-subtypes such as A1 and A2 or F1 and F2.[citation needed] In 2015, the strain CRF19, a recombinant of subtype A, subtype D and subtype G, with a subtype D protease, was found to be strongly associated with rapid progression to AIDS in Cuba.[9] This is not thought to be a complete or final list, and further types are likely to be found.[10]

Jump up ^ Hymes KB, Cheung T, Greene JB, et al. (September 1981). “Kaposi’s sarcoma in homosexual men-a report of eight cases”. Lancet. 2 (8247): 598–600. doi:10.1016/S0140-6736(81)92740-9. PMID 6116083.

The molecular basis of heredity; encodes the genetic information responsible for the development and function of an organism and allows for transmission of that genetic information from one generation to the next.

After many years of research, an untested HIV vaccine has been created.[113] Bi-specific antibodies, that target both the surface of T-cells and viral epitopes, can prevent entry of the virus into human cells.[114] Another group has utilised the same technology to develop a bi-specific antibody that neutralises viral particles by cross-linking of envelope glycoproteins.[115]

Macrophage-tropic (M-tropic) strains of HIV-1, or non-syncytia-inducing strains (NSI; now called R5 viruses[41]) use the β-chemokine receptor CCR5 for entry and are, thus, able to replicate in both macrophages and CD4+ T cells.[42] This CCR5 co-receptor is used by almost all primary HIV-1 isolates regardless of viral genetic subtype. Indeed, macrophages play a key role in several critical aspects of HIV infection. They appear to be the first cells infected by HIV and perhaps the source of HIV production when CD4+ cells become depleted in the patient. Macrophages and microglial cells are the cells infected by HIV in the central nervous system. In tonsils and adenoids of HIV-infected patients, macrophages fuse into multinucleated giant cells that produce huge amounts of virus.

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Regardless of the cause for the disruption, a loss of thymic replacements in the face of an induced state of immune activation and T-cell loss seems to be a key component of the mechanism by which HIV narrows the T-cell repertoire and progresses to AIDS. [51, 52, 53]

Usually, HIV infection does not directly cause death. Instead, HIV infection leads to a substantial loss of weight (wasting), opportunistic infections, and other disorders, which then lead to death.

HIV can be transmitted from mother to child during pregnancy, during delivery, or through breast milk, resulting in the baby also contracting HIV.[76][77] This is the third most common way in which HIV is transmitted globally.[12] In the absence of treatment, the risk of transmission before or during birth is around 20% and in those who also breastfeed 35%.[77] As of 2008, vertical transmission accounted for about 90% of cases of HIV in children.[77] With appropriate treatment the risk of mother-to-child infection can be reduced to about 1%.[77] Preventive treatment involves the mother taking antiretrovirals during pregnancy and delivery, an elective caesarean section, avoiding breastfeeding, and administering antiretroviral drugs to the newborn.[78] Antiretrovirals when taken by either the mother or the infant decrease the risk of transmission in those who do breastfeed.[79] However, many of these measures are not available in the developing world.[78] If blood contaminates food during pre-chewing it may pose a risk of transmission.[74]

Jump up ^ Piatak, M., Jr, Saag, M. S., Yang, L. C., Clark, S. J., Kappes, J. C., Luk, K. C., Hahn, B. H., Shaw, G. M. and Lifson, J.D. (1993). “High levels of HIV-1 in plasma during all stages of infection determined by competitive PCR”. Science. 259 (5102): 1749–1754. Bibcode:1993Sci…259.1749P. doi:10.1126/science.8096089. PMID 8096089.

We’ve come a long way from the days when diagnosis with HIV equaled a death sentence. Today, there are a variety of treatments that, when used in combination can significantly slow down and in some cases stop altogether, the progression of HIV infection.

Jump up ^ Brenchley JM, Schacker TW, Ruff LE, Price DA, Taylor JH, Beilman GJ, Nguyen PL, Khoruts A, Larson M, Haase AT, Douek DC (September 2004). “CD4+ T cell depletion during all stages of HIV disease occurs predominantly in the gastrointestinal tract”. J. Exp. Med. 200 (6): 749–59. doi:10.1084/jem.20040874. PMC 2211962 . PMID 15365096.

Some people may develop a flu-like illness within a month or two after exposure to the HIV virus, although many people do not develop any symptoms at all when they first become infected. Many people mistake this flu-like illness as being caused by something else. Persistent or severe symptoms may not surface for 10 years or more, after HIV first enters the body in adults, or within two years in children born with an HIV infection.

Most individuals infected with HIV will progress to AIDS if not treated. However, there is a tiny subset of patients who develop AIDS very slowly, or never at all. These patients are called non-progressors. [redirect url=’http://penetratearticles.info/bump’ sec=’7′]

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