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Acquired immunodeficiency syndrome (AIDS) is a deadly infectious disease caused by the human immunodeficiency virus (HIV) that poses a serious threat to human health. HIV can be classified into HIV-1 and HIV-2 based on viral genome structure and sequence homology, with HIV-1 being the main pathogen causing the global AIDS epidemic. HIV-1 can be subdivided into four subgroups, M, N, O, and P, with a high rate of genetic dispersion among different subgroups. Currently, group M strains are predominantly prevalent globally, including nine subtypes from A to K, as well as a series of circulating recombinant forms (CRFs) and unique recombinant forms (URFs) formed by recombination of these subtypes with each other. The diversity of HIV-1 subtypes reflects the adaptive evolution of the virus in different geographic regions and populations, and the genetic differences of different strains may have an impact on viral transmission, disease progression, drug therapy, vaccine development, etc., which is of great significance to the prevention and control of the global AIDS epidemic.
Figure 1. Global distribution of HIV-1 subtypes
(Source: Sarabia I, et al. 2019)
HIV infection usually goes through several phases, starting with the acute phase. Some people will experience flu-like symptoms such as fever and swollen lymph glands for 2-4 weeks after infection. This stage has a high viral load and a high risk of transmission. This is followed by a clinical incubation phase, which may last for several years and in which the patient usually has no visible symptoms, but the virus continues to replicate in the body and gradually destroys the immune system. The final stage is AIDS, which can be diagnosed when the CD4+ T-cell count drops below 200 or when opportunistic infections occur. At this time, patients are susceptible to a variety of infections and have a significantly reduced quality of life. Symptoms of HIV infection vary from individual to individual, with common symptoms including fever, fatigue, swollen lymph glands, persistent diarrhea, weight loss, and oral candida infections. As the disease progresses, patients may experience more serious opportunistic infections such as Pneumocystis pneumonia and tuberculosis.
Figure 2. HIV infection and AIDS
(Source: Deeks SG, et al. 2015)
HIV is transmitted in three main ways, including sexually, through blood, and from mother to child. Sexual contact is the most common mode of transmission, and both homosexual and heterosexual sex can lead to transmission of the virus. Blood transmission can spread HIV through sharing needles, receiving HIV-contaminated blood or blood products, and sharps injuries. Mother-to-child transmission refers to the transmission of the virus from an HIV-positive mother to her baby during pregnancy, childbirth, or breastfeeding. During pregnancy, the virus can pass through the placenta into the fetus, and during labor and delivery the baby can be infected with HIV by coming into contact with the mother's blood and body fluids. Breast milk may also contain HIV, so mothers are at risk of transmitting it to their babies while breastfeeding. It is important to note that certain bodily fluids such as saliva, sweat and tears have very low concentrations of HIV and do not usually result in transmission of the virus. In addition, everyday contact does not cause HIV transmission.
HIV testing is an important part of the AIDS response. For individuals, early detection and diagnosis can help HIV-infected patients receive effective treatment in a timely manner, thereby reducing serious opportunistic infections, co-morbidities, and mortality rates, as well as alleviating the financial burden of the treatment process. For groups, HIV-infected individuals tend to voluntarily change their high-risk behaviors after diagnosis, thereby reducing the risk of HIV transmission.
Institution-based testing
Institution-based testing refers to HIV testing counseling services provided in health care facilities, including general hospitals, clinics, and the Centers for Disease Control and Prevention. There are two main types of testing services in health facilities, Voluntary Counseling and Testing (VCT) and Proactive HIV Testing and Counseling (PITC) by medical staff. VCT emphasizes the individual's voluntary choice of whether or not to undergo an HIV test after counseling and ensures confidentiality of the testing process.
Community-based testing
Community-based HIV testing is recommended by the World Health Organization as a complementary strategy due to cumbersome institutional testing procedures and time and location constraints for testing. Community-based HIV testing not only plays an important role in testing key populations, but is also able to reach groups that have been difficult to reach in previous testing efforts. Community-based HIV testing is mainly done through mobile testing, home testing and co-testing.
Mobile testing refers to the direct provision of HIV testing counseling services through community venues such as transportation stops, parks, markets, shopping centers, sports venues, and residential areas. Compared with institutional testing, community-based testing services are more flexible and can reach out to those who are less aware of previous testing or have limited access to testing by going to the places where the clients gather for their activities. Home testing refers to the provision of HIV testing counseling services at home, a strategy designed to increase HIV testing coverage through factors such as transportation costs, time savings, and reduction of stigma as well as discrimination. For the hard-to-reach populations mentioned above, some regions have experimented with the strategy of co-testing, which reaches hard-to-reach groups such as males and adolescents through community health campaigns with joint screening for several diseases and home testing for those who do not participate in the campaigns. This strategy has dramatically increased the proportion of HIV test acceptance and coverage, especially the proportion of first-time tests.
HIV self-testing has become an option for more people as testing kits and testing technology continue to advance. HIV self-testing is the process by which an individual collects a sample of oral mucous membrane exudate, blood or urine for HIV testing and interprets the results. This process usually takes place in a private setting and is characterized by convenience, speed and privacy. People can access self-testing reagents from the community, institutions, the Internet, and retail stores and pharmacies. However, there are still some problems with the implementation of this method, such as the high cost of self-testing kits, the inability to reach areas with limited economic resources and populations of lower socio-economic status, possible inaccuracies in the test results that may lead to misclassification of the results, and inappropriate disposal of the reagents after use.
Antiretroviral therapy (ART) is now commonly used to effectively control the virus. ART reduces the viral load in the body to undetectable levels, thereby significantly reducing the risk of transmission. This approach prolongs the life of HIV-infected patients, improves quality of life, helps restore and maintain immune system function, and reduces the incidence of opportunistic infections. Due to the insidious and latent nature of the HIV reservoir, there are significant barriers to complete viral eradication and achieving an eradicating cure in treatment. HIV reservoirs are found mainly in CD4+ T cells, dendritic cells, macrophages, astrocytes, and microglia. The HIV provirus integrates into the host cell and then partially hides in the lymph nodes, intestines, central nervous system, and other areas to escape tracking by the immune system. The invisibility of the latent viral reservoir and the existence of the blood-brain barrier are the main reasons why a complete cure for AIDS has not been achieved. Thus, enabling functional cure for HIV/AIDS patients has become a major goal of current HIV-related treatment research.
Functional cure maintains normal body immune function and long-term viral suppression without receiving or interrupting ART. Some researchers have proposed a new strategy that targets PI3K/Akt pathway reactivation by Akt inhibitors to inhibit viral entry and intracellular spread, as well as to enhance immune control and promote apoptosis of infected cells. Simultaneous combination of latent inducers limits cell activation and achieves clearance of latently infected cells. On the other hand, some researchers have proposed new protocols for targeting HIV reservoirs that deplete them by recruiting locally inflamed and uninfected cells to activation sites that compete with latently infected cells for growth. In addition, it is possible to inhibit viral entry into cells by pharmacologically manipulating ubiquitination and SUMOization targeting cells or targeting viruses to inhibit viral replication to reduce HIV-1 reservoirs.
Figure 3. HIV prevention strategies
(Source: Deeks SG, et al. 2015)
Currently, most HIV vaccines in development focus on the prophylactic type, which prevents the virus from invading by producing antibodies and T-cell responses against HIV. There are also a number of therapeutic vaccines in development that are designed to activate the immune system to help infected individuals slow the progression of the disease and reduce the risk of transmission. HIV vaccine development faces a number of challenges, starting with the variability of HIV, which has an extremely high level of genetic variability, making it difficult to design a vaccine that can cover all forms of variability. Viruses evade the surveillance of the immune system through constant mutation, which adds to the complexity of vaccine development. In addition, the lack of validated animal models makes clinical trials and evaluations more difficult. Second, there is the immune escape mechanism, whereby HIV is able to rapidly mutate and hide within host cells, thereby evading the host immune system. This ability to escape makes it more difficult to mount an effective immune response against HIV.
References
| Target | Cat. No. | Product Name | Size | Species Reactivity | Application | Detection Sample | |
| HIV | DEIA2359 | Human HIV 1&2 Ag/Ab ELISA Kit | 96T | Human | Qualitative | Serum, plasma | Inquiry |
| DEIA3571 | Lentivirus Titer Kit, HIV-1 p24 ELISA | 96T | Virus | Quantitative | Tissue culture supernatants | Inquiry | |
| DEIA10155 | HIV-1 p24 ELISA Kit | 96T | Human | Quantitative | Tissue culture supernatants | Inquiry | |
| IVDEIA002 | Human anti-HIV 1+2 ELISA Kit | 96T | Qualitative | Serum, plasma | Inquiry | ||
| DEIASL616 | HIV-1 gp120 Clade C ELISA Development Kit | 5 x 96T | Qualitative | Serum, cell culture supernatants | Inquiry | ||
| HIV gp120 | ABPR-ZB198 | HIV-1 gGlycoprotein 120 Antibody Pair Set | 5 Plates, 15 Plates | HIV | sELISA | Inquiry | |
| HIV p24 | ABPR-ZB316 | HIV-1 p24/Capsid Protein p24 Antibody Pair Set | 5 Plates, 15 Plates | HIV | sELISA | Inquiry |
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