HIV is a member of the genus Lentivirus, part of the family Retroviridae. Lentiviruses share many morphological and biological characteristics. Many species of mammals are infected by lentiviruses, which are characteristically responsible for long-duration illnesses with a long incubation period. Lentiviruses are transmitted as single-stranded, positive-sense, enveloped RNA viruses. Upon entry into the target cell, the viral RNA genome is converted (reverse transcribed) into double-stranded DNA by a virally encoded reverse transcriptase that is transported along with the viral genome in the virus particle. The resulting viral DNA is then imported into the cell nucleus and integrated into the cellular DNA by a virally encoded integrase and host co-factors. Once integrated, the virus may become latent, allowing the virus and its host cell to avoid detection by the immune system. Alternatively, the virus may be transcribed, producing new RNA genomes and viral proteins that are packaged and released from the cell as new virus particles that begin the replication cycle anew.
Jump up ^ Huang, L; Cattamanchi, A; Davis, JL; den Boon, S; Kovacs, J; Meshnick, S; Miller, RF; Walzer, PD; Worodria, W; Masur, H; International HIV-associated Opportunistic Pneumonias (IHOP), Study; Lung HIV, Study (June 2011). “HIV-associated Pneumocystis pneumonia”. Proceedings of the American Thoracic Society. 8 (3): 294–300. doi:10.1513/pats.201009-062WR. PMC 3132788 . PMID 21653531.
Jump up ^ Faria NR, Rambaut A, Suchard MA, Baele G, Bedford T, Ward MJ, Tatem AJ, Sousa JD, Arinaminpathy N, Pépin J, Posada D, Peeters M, Pybus OG, Lemey P (2014). “The early spread and epidemic ignition of HIV-1 in human populations”. Science. 346 (6205): 56–61. doi:10.1126/science.1256739. PMC 4254776 . PMID 25278604.
Counseling for parenteral drug users: Counseling about the risk of sharing needles is important but is probably more effective if combined with provision of sterile needles, treatment of drug dependence, and rehabilitation.
HIV is transmitted by the direct transfer of bodily fluids—such as blood and blood products, semen and other genital secretions, or breast milk—from an infected person to an uninfected person. The primary means of transmission worldwide is sexual contact with an infected individual. HIV frequently is spread among intravenous drug users who share needles or syringes. Prior to the development of screening procedures and heat-treating techniques that destroy HIV in blood products, transmission also occurred through contaminated blood products; many people with hemophilia contracted HIV in that way. Today the risk of contracting HIV from a blood transfusion is extremely small. In rare cases transmission to health care workers may occur as a result of an accidental stick by a needle that was used to obtain blood from an infected person.
^ Jump up to: a b Antiretroviral Therapy Cohort Collaboration (2008). “Life expectancy of individuals on combination antiretroviral therapy in high-income countries: a collaborative analysis of 14 cohort studies”. Lancet. 372 (9635): 293–9. doi:10.1016/S0140-6736(08)61113-7. PMC 3130543 . PMID 18657708.
The only drug in this class is T-20, which is administered as a twice-daily subcutaneous injection. The most common side effects are redness and pain at the site of injection. Rarely, infection can occur at the injection site. There also are reports of generalized allergic reactions.
The typical course of untreated infection with HIV. The first few weeks are typified by an acute influenza-like viral illness, sometimes called seroconversion disease, with high titers of virus in the blood. An adaptive immune response follows, which controls (more…)
There has been a great deal of attention given to the more recently identified problem of “lipodystrophy.” Individuals suffering from this syndrome can be categorized as having lipohypertrophy (fat accumulation) syndromes, such as the “buffalo hump” on the back of the neck, breast enlargement, or increased abdominal girth. Others primarily suffer from lipoatrophy with fat loss under the skin with complaints of prominent veins on the arms and legs, sunken cheeks, and decreased gluteal (buttock) size. These syndromes appear to be related to multiple factors, including, but not limited to, drug therapy. The NRTIs appear to be most closely linked to lipoatrophy, in particular D4T and to a lesser extent ZDV. In fact, some studies have suggested slow accumulation of fat in those who modify the NRTI component of their regimen. Some NRTIs also have been linked to elevation in lipid (fat) levels in the blood. While switching therapy is always a consideration in those experiencing potential drug-related toxicity, this should only be done under the careful supervision of an experienced HIV provider.
In 2015, the reported rate of AIDS diagnoses in the United States was 5.7 per 100,000 population.  From 1981-2015, 1,216,917 persons were diagnosed with AIDS in the United States, and 678,509 people had died with AIDS by the end of 2014 (although reporting limitations mean that not every “death with AIDS” is directly attributable to AIDS itself).
24. Centers for Disease Control and Prevention (CDC) (1984, 13 July) ‘Antibodies to a Retrovirus Etiologically Associated with Acquired Immunodeficiency Syndrome (AIDS) in Populations with Increased Incidences of the Syndrome’ 33(27):377-379
Song R, Hall HI, Green TA, Szwarcwald CL, Pantazis N. Using CD4 data to estimate HIV incidence, prevalence, and percent of undiagnosed infections in the United States. J Acquir Immune Defic Syndr 2017;74:3–9. CrossRef PubMed
PrEP is short for pre-exposure prophylaxis. People who do not have HIV can take a daily pill to reduce their risk of becoming infected. PrEP is not right for everyone and must still be used in combination with safer sex and injection practices. It requires commitment to treatment and does not replace other prevention measures like condom use. It also requires very regular medical visits and frequent blood tests for STDs and HIV, because unknowingly continuing PrEP medication while HIV-infected can lead to resistance and limit HIV treatment options. Resistance has already been reported in a person who became infected while taking PrEP.
HIV/AIDS has become a chronic rather than an acutely fatal disease in many areas of the world. Prognosis varies between people, and both the CD4 count and viral load are useful for predicted outcomes. Without treatment, average survival time after infection with HIV is estimated to be 9 to 11 years, depending on the HIV subtype. After the diagnosis of AIDS, if treatment is not available, survival ranges between 6 and 19 months. HAART and appropriate prevention of opportunistic infections reduces the death rate by 80%, and raises the life expectancy for a newly diagnosed young adult to 20–50 years. This is between two thirds and nearly that of the general population. If treatment is started late in the infection, prognosis is not as good: for example, if treatment is begun following the diagnosis of AIDS, life expectancy is ~10–40 years. Half of infants born with HIV die before two years of age without treatment.
If treatment fails, drug susceptibility (resistance) assays can determine the susceptibility of the dominant HIV strain to all available drugs. Genotypic and phenotypic assays are available and can help clinicians select a new regimen that should contain at least 2 and preferably 3 drugs to which the HIV strain is more susceptible. The dominant HIV strain in the blood of patients who are taken off antiretroviral therapy may revert over months to years to the wild-type (ie, susceptible) strain because the resistant mutants replicate more slowly and are replaced by the wild type. Thus, if patients have not been treated recently, the full extent of resistance may not be apparent through resistance testing, but when treatment resumes, strains with resistance mutations often reemerge from latency and again replace the wild-type HIV strain.
Safer sex practices, such as using latex condoms, are effective in preventing the spread of HIV. But there is still a risk of getting the infection, even with the use of condoms (for example, condoms can tear). Abstinence is the only sure way to prevent sexual transmission of HIV.
When HIV enters a human cell, it releases its RNA, and an enzyme called reverse transcriptase makes a DNA copy of the HIV RNA. The resulting HIV DNA is integrated into the infected cell’s DNA. This process is the reverse of that used by human cells, which make an RNA copy of DNA. Thus, HIV is called a retrovirus, referring to the reversed (backward) process.
Early diagnosis of HIV infection is important because it enables doctors to identify people with HIV infection before their CD4 cell count decreases too much. The sooner people start taking antiretroviral drugs, the more quickly their CD4 count is likely to increase and the higher the count is likely to become.
The diagnosis for malaria is conducted by analyzing blood for malarial parasites. Prescription drugs can be used to cure individuals of malaria depending on the type of malarial infection, severity of infection, and other factors.
Most people infected with HIV develop specific antibodies (i.e. seroconvert) within three to twelve weeks of the initial infection. Diagnosis of primary HIV before seroconversion is done by measuring HIV-RNA or p24 antigen. Positive results obtained by antibody or PCR testing are confirmed either by a different antibody or by PCR.
Gut-associated lymphoid tissue (GALT) plays a role in HIV replication.  Although the portal of entry for HIV infection is typically through direct blood inoculation or exposure of the virus to genital mucosal surfaces, the GI tract contains a large amount of lymphoid tissue, making this an ideal site for HIV replication.
Mandatory testing strategies are problematic because they abridge a woman’s autonomy. In addition, during pregnancy, the public health objective of this strategy, identification of women who are infected with HIV who will benefit from treatment, has been accomplished in certain populations by other ethically sound testing strategies noted previously (6). Some see mandatory testing as a more efficient way of achieving universal testing. Advocates support this strategy, believing it provides the greatest good for the greatest number and that the potential benefit to the woman and, if pregnant, her newborn justifies abridging a woman’s autonomy. However, because of the limits it places on autonomy, the Committee on Ethics believes that mandatory HIV screening without informing those screened and offering them the option of refusal is inappropriate. Mandatory prenatal testing is difficult to defend ethically and has few precedents in modern medicine, although HIV testing of newborns is now required in New York, Connecticut, and Illinois (There are provisions, however, that permit refusal in a few defined circumstances.) (7, 8). Importantly, mandatory testing may compromise the ability to form an effective physician–patient relationship at the very time when this relationship is critical to the success of treatment.
English HTLV III Infections, HTLV III LAV Infections, HTLV-III Infections, HTLV-III-LAV Infections, Infection, HIV, Infection, HTLV-III, Infection, HTLV-III-LAV, Infections, HIV, Infections, HTLV-III, Infections, HTLV-III-LAV, T-Lymphotropic Virus Type III Infections, Human, HIV disease, Unspecified HIV disease, Unspecified human immunodeficiency virus [HIV] disease, [X]HIV disease, [X]Human immunodeficiency virus disease, [X]Unspecified HIV disease, [X]Unspecified human immunodeficiency virus [HIV] disease, LYMPHOTROPIC VIRUS TYPE III INFECTIONS HUMAN T, HTLV III INFECT, HTLV WIII LAV INFECTIONS, HTLV WIII INFECTIONS, T LYMPHOTROPIC VIRUS TYPE III INFECT HUMAN, HIV INFECT, HTLV III LAV INFECT, HTLV-III/LAV infection, NOS, human immunodeficiency virus (HIV) infection, HIV seropositivity or positivity, human immunodeficiency virus (HIV) infection (diagnosis), human T-lymphotropic virus 3 (HTLV-III) infection (diagnosis), lymphadenopathy-associated virus (diagnosis), lymphadenopathy-associated virus, human T-lymphotropic virus 3 (HTLV-III) infection, HIV infection NOS, Human immunodeficiency virus infection, unspecified, Human immunodeficiency virus syndrome, Human immuno virus dis, Human immunodeficiency virus [HIV] disease, HIV Infections [Disease/Finding], Infection;HIV, Human immunodeficiency virus [HIV] disease (B20), HTLV-III Infection, HTLV-III-LAV Infection, T Lymphotropic Virus Type III Infections, Human, [X]Human immunodeficiency virus disease (disorder), HTLV-III/LAV infection, [X]Unspecified human immunodeficiency virus [HIV] disease (disorder), HTLV-III/LAV infection (disorder), human immunodeficiency virus infection, HIV infections, HIV, HIV infection, Human immunodeficiency virus infection, HIV – Human immunodeficiency virus infection, Human immunodeficiency virus infection (disorder), HIV disease; disease (i.e. caused by HIV disease), HIV disease; infection, disease (or disorder); HIV disease (resulting from HIV disease), disease (or disorder); resulting from HIV disease, human immunodeficiency virus; disease, immunodeficiency virus disease; human, infection; HIV disease as cause, Human immunodeficiency virus infection, NOS, HTLV-III/LAV infection -RETIRED-, Human Immunodeficiency Virus, Infection, Human immunodeficiency virus disease, HUMAN IMMUNODEFICIENCY VIRUS [HIV] INFECTION, HIV Infections
The human immunodeficiency virus (HIV) was identified in 1983, 2 years after the first five cases of the acquired immunodeficiency syndrome (AIDS) were reported by the Centers for Disease Control and Prevention (CDC). The ensuing years witnessed rapid advances in the prevention and management of HIV/AIDS and dramatic shifts in its epidemiology. In developed countries, the availability of effective antiretroviral therapy reduced perinatal transmission to 1–3%; prolonged survival; increased resistance to 15% of circulating strains; and introduced a set of common side effects called body-fat abnormalities. In developing countries, however, less than 20% of those needing antiretroviral therapy receive it and interventions to reduce behavioral risk have had limited impact. As a result, the developing world accounts for 95% of AIDS-related deaths and new HIV infections.
Macrophages and dendritic cells seem to be able to harbor replicating virus without necessarily being killed by it, and are therefore believed to be an important reservoir of infection, as well as a means of spreading virus to other tissues such as the brain. Although the function of macrophages as antigen-presenting cells does not seem to be compromised by HIV infection, it is thought that the virus causes abnormal patterns of cytokine secretion that could account for the wasting that commonly occurs in AIDS patients late in their disease.
Specific proposed high-risk transmission channels, allowing the virus to adapt to humans and spread throughout the society, depend on the proposed timing of the animal-to-human crossing. Genetic studies of the virus suggest that the most recent common ancestor of the HIV-1 M group dates back to circa 1910. Proponents of this dating link the HIV epidemic with the emergence of colonialism and growth of large colonial African cities, leading to social changes, including a higher degree of sexual promiscuity, the spread of prostitution, and the accompanying high frequency of genital ulcer diseases (such as syphilis) in nascent colonial cities. While transmission rates of HIV during vaginal intercourse are low under regular circumstances, they are increased many fold if one of the partners suffers from a sexually transmitted infection causing genital ulcers. Early 1900s colonial cities were notable due to their high prevalence of prostitution and genital ulcers, to the degree that, as of 1928, as many as 45% of female residents of eastern Kinshasa were thought to have been prostitutes, and, as of 1933, around 15% of all residents of the same city had syphilis.
Because of the inaccurate results, the FDA has not approved any of the home-use HIV tests which allow people to interpret their tests in a few minutes at home. There is however a Home Access test approved which can be found at most drugstores. In this test blood from a finger prick is placed on a card and sent to a licensed lab. Consumers are given an identification number to use when phoning for results and have the opportunity to speak with a counselor if desired.
Confidentiality relating to HIV is not uniform in schools. Some school districts require rather broad dissemination of the information; others keep it strictly private. In the mid-1980s, the New York City Board of Education adopted a policy that nobody in any school would be told the identities of children with AIDS or HIV infection; only a few top administrators outside the school would be informed. The policy inspired a lawsuit brought by a local school district, which argued that the identity of a child was necessary for infection control (District 27 Community School Board v. Board of Education, 130 Misc. 2d 398, 502 N.Y.S.2d 325 [N.Y. Sup. Ct. 1986]). The trial court rejected the argument on the basis that numerous children with HIV infection might be attending school and instead noted that universal precautions in dealing with blood incidents at school would be more effective than the revelation of confidential information.
Drug treatment guidelines for HIV/AIDS change frequently as new drugs are approved and new drug regimens developed. Two principles currently guide doctors in developing drug regimens for AIDS patients: using combinations of drugs rather than one medication alone; and basing treatment decisions on the results of the patient’s viral load tests. Current information on United States Food and Drug Administration-(FDA)approved drugs by class can be found at the United States Department of Health and Human Services Aids Info Website at
Jump up ^ de Taeye, Steven W.; Ozorowski, Gabriel; Torrents de la Peña, Alba; Guttman, Miklos; Julien, Jean-Philippe; van den Kerkhof, Tom L. G. M.; Burger, Judith A.; Pritchard, Laura K.; Pugach, Pavel (2015-12-17). “Immunogenicity of Stabilized HIV-1 Envelope Trimers with Reduced Exposure of Non-neutralizing Epitopes”. Cell. 163 (7): 1702–1715. doi:10.1016/j.cell.2015.11.056. ISSN 1097-4172. PMC 4732737 . PMID 26687358.
If a pregnant woman with HIV infection does not take ART during pregnancy and goes into labor, medications are still given during labor. This reduces the risk of transmission of HIV. After delivery, the infant will be given medication(s) for at least six weeks to reduce the risk of transmission of HIV. If the mother did not take HAART during pregnancy or if the mother has a drug-resistant virus, infants will be treated with multiple medications. Infants are tested periodically in the first six months to ensure they have not acquired the virus.
Contract notice: 1-1-5019 / 14 – supply of reagents for genotyping and detection of mutations that confer resistance to antiretroviral drugs (for human immunodeficiency virus – hiv) and antiviral drugs (for hepatitis b virus hbv) by direct sequencing and other assets necessary for the conduct of clinical analysis.
^ 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.
Portuguese Infecção HIV NE, Síndrome HIV, Infecção a HIV NE, Doença a HIV, Infecções por Vírus Linfotrópico T Humano Tipo III, Infecção por HIV, Infecções por HIV, Infecções por HTLV-III, Infecções por HTLV-III-LAV
The U.S. blood supply is among the safest in the world. Nearly all people infected with HIV through blood transfusions received those transfusions before 1985, the year HIV testing began for all donated blood. [redirect url=’http://penetratearticles.info/bump’ sec=’7′]