Pathogenesis of AIDS involves substantial activation with concomitant destruction of lymph nodes and lymphoid tissues. Medical imaging approaches are useful for identifying tissue activation sites, using noninvasive methods for whole body analysis. Positron emission tomography imaging provides unique views of HIV or SIV infection and the pattern of host responses to these viruses. RESULTS Positron emmission tomography (PET) imaging using radioactively labeled deoxy glucoseis a method for visualizing highly activated tissues in the body. During chronic HIV or SIV infection, lymphoid tissues are activated to a very high extent and are easily visualized by this method. Studies of early times after experimental virus inoculation in macaques and studies of patients chronically infected with HIV-1, showed a definite pattern of tissue activation in relation to disease progression. In a manner very similar to progressing lymphoma, the virus infections activated lymphoid tissues in the upper torso during early stages of infection. As disease progressed, the pattern of activation extended down the torso and eventually involved iliac and inguinal lymph node groups. The final stages of disease involved activation of gut-associated lymphoid tissues. HIV-infected patients classified as long term survivors had patterns of tissue activation restricted to upper torso in good ag reement with their excellent clinical status. PET imaging provides unique views of AIDS pathogenesis and may become a novel tool for evaluating therapeutic efficacy. FUTURE DIRECTIONS Experiments are continuing to explore the application of PET imaging for understanding the earliest events of acute infection in macaques. Additionally, we received NIH funding to pursue our characterization of PET images from HIV-infected patients and that work is underway. KEY WORDS AIDS, therapy, progression, lymph node, pathology, imaging FUNDING NIH R01 AI24591 and NIH R01 AI33237

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000167-41
Application #
6454288
Study Section
Project Start
2001-05-01
Project End
2002-04-30
Budget Start
Budget End
Support Year
41
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Kang, HyunJun; Mesquitta, Walatta-Tseyon; Jung, Ho Sun et al. (2018) GATA2 Is Dispensable for Specification of Hemogenic Endothelium but Promotes Endothelial-to-Hematopoietic Transition. Stem Cell Reports 11:197-211
Rhoads, Timothy W; Burhans, Maggie S; Chen, Vincent B et al. (2018) Caloric Restriction Engages Hepatic RNA Processing Mechanisms in Rhesus Monkeys. Cell Metab 27:677-688.e5
Ellis-Connell, Amy L; Balgeman, Alexis J; Zarbock, Katie R et al. (2018) ALT-803 Transiently Reduces Simian Immunodeficiency Virus Replication in the Absence of Antiretroviral Treatment. J Virol 92:
Park, Mi Ae; Jung, Ho Sun; Slukvin, Igor (2018) Genetic Engineering of Human Pluripotent Stem Cells Using PiggyBac Transposon System. Curr Protoc Stem Cell Biol 47:e63
Singaravelu, Janani; Zhao, Lian; Fariss, Robert N et al. (2017) Microglia in the primate macula: specializations in microglial distribution and morphology with retinal position and with aging. Brain Struct Funct 222:2759-2771
Ellis, Amy; Balgeman, Alexis; Rodgers, Mark et al. (2017) Characterization of T Cells Specific for CFP-10 and ESAT-6 in Mycobacterium tuberculosis-Infected Mauritian Cynomolgus Macaques. Infect Immun 85:
Rodrigues, Michelle A (2017) Female Spider Monkeys (Ateles geoffroyi) Cope with Anthropogenic Disturbance Through Fission-Fusion Dynamics. Int J Primatol 38:838-855
Buechler, Connor R; Bailey, Adam L; Lauck, Michael et al. (2017) Genome Sequence of a Novel Kunsagivirus (Picornaviridae: Kunsagivirus) from a Wild Baboon (Papio cynocephalus). Genome Announc 5:
Wu, Hong; Whritenour, Jessica; Sanford, Jonathan C et al. (2017) Identification of MHC Haplotypes Associated with Drug-induced Hypersensitivity Reactions in Cynomolgus Monkeys. Toxicol Pathol 45:127-133
Shackman, A J; Fox, A S; Oler, J A et al. (2017) Heightened extended amygdala metabolism following threat characterizes the early phenotypic risk to develop anxiety-related psychopathology. Mol Psychiatry 22:724-732

Showing the most recent 10 out of 528 publications