Submit Manuscript | http://medcraveonline.com most untreated individuals. Within secondary lymphoid tissues, HIV- 1 replication is highly concentrated in follicular CD4+T cells, 3–10 which are 30-40 times more likely to be productively infected than extra follicular CD4+T cells during chronic HIV-1 infection. 3 Consequently, follicular CD4+T cells account for approximately 70% of HIV-1 producing cells in chronic disease prior to AIDS. 3,4 Follicular dendritic cells (FDC) located in germinal centers of follicles, bind HIV-antibody complexes, and these complexes readily infect CD4+T cells in vitro, 11 thus providing an explanation for the high rate of infection of follicular CD4+T cells. Nevertheless, it is unclear why HIV-1-specifc CD8+T cells are unable to fully suppress HIV-1 replication in follicular CD4+T cells, as they are able to kill productively infected cells in vitro within minutes after they initiate transcription of virus and long before infectious virions are produced. Multiple lines of evidence indicate that HIV-1-specifc CD8+T cells play a pivotal role in controlling virus replication. Development of HIV-1-specifc CD8+T cells during acute infection coincides with declines in viremia 12–14 suggesting that CTL are critical determinants of the initial control of virus replication. In the SIV-infected rhesus macaque model of HIV-1, temporary removal of CD8+T cells leads to increased viremia, and the subsequent return of CD8+T cells correlates with decreased viremia, 15,16 further implicating CD8+T cells in viral control. Levels of polyfunctional CD8+T cells inversely correlate with virus set point 17 and polyfunctional CD8+T cells are maintained in HIV-1 infected nonprogressors. 18 Furthermore, there is a strong association of MHC class-I alleles with particular outcomes of HIV-1 and SIV infections, 19 and it is hypothesized that this is related to the effciency of virus-specifc CTL responses. The CD8+T cell response to HIV-1 is unique because in some cases virus-specifc cytolysis is detectable in PBMC in the absence of in vitro stimulation, 20,21 a phenomenon that has not been frequently reported in other chronic viral infections. Nevertheless, despite evidence that HIV-1-specifc CD8+T cells are abundant and capable of cytolytic function, they are unable to fully suppress virus replication in vivo resulting in the progressive depletion of CD4+T cells and, ultimately, death in untreated individuals. Quite perplexingly as well, in multiple studies the administration of exogenous CD8+T cells has failed to result in signifcant decreases in plasma HIV-1 RNA concentrations. 22–25 Furthermore, increases in HIV-specifc CTL through therapeutic vaccination or treatment interruption have resulted in little or no enhancement of virologic control. 26–29 HIV-1 evades HIV-1-specifc CD8+T cells through multiple mechanisms, which likely contribute to the inability of HIV-1-specifc CTL to fully control HIV-1 replication. First, HIV-1 latently infected cells do not express viral proteins, which are essential to CD8+T cell recognition. Second, HIV-1 frequently mutates to evade CD8+T cell responses. 19 Third, HIV-specifc CD8+T cells fail to accumulate in lymphoid B cell follicles and are not able to effectively clear the follicular reservoir of HIV-1-producing cells 3 (Figure 1). This might explain why individuals with functional HIV-specifc CD8+T cells fail to fully suppress HIV-1 replication, and why infused exogenous CD8+T cells or augmented endogenous CTL responses failed to signifcantly impact viral control. Future HIV-1 cure and vaccine strategies must address not only the latent reservoir of HIV-1 infected cells and HIV-specifc CD8+T cell escape mutations, but also the reservoir of HIV-1 producing cells within B cell follicles. Strategies to induce follicular lysis, such as through administration of the B-cell depleting monoclonal antibody rituximab, might temporarily allow virus-specifc CTL to access the follicles. However, this would profoundly impair humoral immunity, and furthermore, the effects would only be transient. Once the B cell population recovered and follicles were reconstituted, HIV-1 replication most likely would resume at that site. Perhaps a better approach to eradicate the reservoir of HIV-1 within follicles, and one that we are presently developing, 30 is to engineer functional HIV-1- specifc CD8+T cells to express chemokine receptors, such as the follicular homing molecule CXCR5, to allow virus-specifc CTL to access the follicular compartment and clear the reservoir of HIV-1 producing cells within follicles. This approach could be applied by itself or in conjunction with other approaches such as one to stimulate latently infected cells to express HIV-1. Additionally, this approach could be implemented using CD8+T cells directed against HIV-1 neo- epitopes, 19 in cases where HIV-specifc CD8+T cell escape mutations are an issue. Ultimately, therapeutic approaches that enable HIV- specifc CD8+T cells to enter lymphoid B cell follicles and clear HIV- 1 producing cells may lead to a functional cure for HIV-1. J Hum Virol Retrovirol. 2014;1(1):1‒3. 1 © 2014 Skinner et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and build upon your work non-commercially. Overcoming the immune privilege of B cell follicles to cure HIV-1 infection Volume 1 Issue 1 - 2014 Pamela J Skinner, 1 Elizabeth Connick 2 1 Department of Veterinary and Biomedical Sciences, University of Minnesota, USA 2 Department of Medicine, University of Colorado Anschutz Medical Campus, USA Correspondence: Pamela J Skinner, University of Minnesota, 1971 Commonwealth Ave, Saint Paul, MN, USA, Tel 612-624- 2644, Email Received: April 17, 2014 | Published: April 24, 2014 Journal of Human Virology & Retrovirology Editorial Open Access Editorial Over 30 million individuals are infected with HIV-1 world-wide. The disease produces great human suffering and extracts an enormous fnancial toll. Although antiretroviral drugs have produced substantial reductions in HIV-1 related morbidity and mortality, they are costly, associated with side effects, and ineffective in the presence of drug resistant virus. Despite intensive efforts, both a protective vaccine and a cure for HIV-1 remain elusive. Ongoing HIV-1 replication despite host immune responses to the virus is an enigma and poses a major barrier to the development of a vaccine or a cure. HIV-1 replication occurs primarily in CD4+T cells within secondary lymphoid tissues 1,2 and results in a progressive decline of CD4+T cells, immunodefciency, and ultimately death in