Full Text PA-96-059 HIV: VIRAL LOAD IN BRAIN AND NEUROBEHAVIORAL CORRELATES NIH Guide, Volume 25, Number 20, June 21, 1996 PA NUMBER: PA-96-059 P.T. 34 Keywords: Infectious Diseases/Agents Neuroscience National Institute of Mental Health National Institute of Neurological Disorders and Stroke PURPOSE It is generally agreed that the presence of HIV within the central nervous system (CNS) contributes to the development of neurobehavioral impairments and neurologic syndromes that occur in a subset of HIV-infected individuals. However, a direct link between the presence of virus and HIV-induced motor/cognitive impairments has yet to be elucidated. This program announcement solicits research applications to (1) identify effective ways to quantitate viral load within the CNS during life; (2) correlate the quantity of virus within the CNS to the onset and course of neurobehavioral and neurological changes; (3) identify specific biochemical or neurochemical alterations in neuronal function as a consequence of the presence of virus either directly or indirectly; and (4) identify and test drugs that prevent or reverse the neuronal dysfunction. Collaborations between neuroscientists and immunologists/virologists are encouraged but not required. Fellowships are also solicited through this program announcement to encourage a broader range of scientists to conduct research in this field. HEALTHY PEOPLE 2000 The Public Health Service (PHS) is committed to achieving the health promotion and disease prevention objectives of "Healthy People 2000," a PHS-led national activity for setting priority areas. This PA, Viral Load in Brain and Neurobehavioral Correlates, is related to the priority areas of mental health and mental disorders. Potential applicants may obtain a copy of "Healthy People 2000" (Full Report: Stock No. 017-001-00474-0 or Summary Report: Stock No. 017-001-00473-1) through the Superintendent of Documents, Government Printing Office, Washington, DC 20402-9325 (telephone 202-512-1800). ELIGIBILITY REQUIREMENTS Eligibility and requirements for different funding mechanisms vary. Applicants are advised to contact NIMH or NINDS program staff listed under INQUIRIES for additional information and specific application procedures. Applications may be submitted by foreign and domestic, for- profit and non-profit organizations, public and private, such as universities, colleges, hospitals, laboratories, units of State and local governments, and eligible agencies of the Federal government. Foreign institutions are not eligible for small grants (R03), First Independent Research Support and Transition (FIRST) (R29) awards, program projects (P01), research career awards (K-series), or fellowships (F-series). Racial/ethnic minority individuals, women, and persons with disabilities are encouraged to apply as Principal Investigators. MECHANISM OF SUPPORT The mechanisms available for support by the NIMH are: research project grants (R01), FIRST awards (R29), program project grants (P01), research career programs (K01, K02, K05), fellowship programs (F30, F31, F32) and small research grants (R03). The mechanisms available for support by the NINDS are: the research projects grants (R01), FIRST Awards (R29), program project grants (P01), and fellowships (F32). Because certain grants have special eligibility requirements, application formats, and review criteria (i.e., small grants and FIRST awards), applicants are strongly encouraged to consult with program staff listed under INQUIRIES and obtain the appropriate additional announcements for those grant mechanisms. RESEARCH OBJECTIVES Central nervous system (CNS) complications occur in a large number of HIV-infected adults and children. This is manifested by both motor and cognitive impairments. Early manifestation of CNS dysfunction include slowed processing, forgetfulness, delayed reaction time, or generalized weakness. In the most severe instances, patients may become demented or exhibit partial to complete motor paralysis. HIV-induced motor/cognitive dysfunction compromises the life of the affected individual. The mechanisms underlying CNS dysfunction are not clear. It is known that HIV enters the CNS early after infection, however neurons appear not to be infected. Instead, virus is found primarily in cells of the monocyte/macrophage lineage. Viral infection of other CNS cells has also been demonstrated, including astrocytes and endothelial cells that make up the blood brain barrier. Indirect effects of the virus are numerous, including, but not limited to, changes in the blood brain barrier, increased cellular trafficking, altered cytokine expression, loss of neurons, and changes in brain size/quality/density reflected in brain images seen by various neuroimaging studies. The direct link between the presence of virus in the brain and the resulting neurobehavioral impairments is not clear. Although virus within the CNS is assumed necessary for CNS disease, measures to quantitate virus within the CNS during life are inadequate. Quantitating viral load in brain tissue at the time of death gives valuable information. However, this state of the brain at end stage disease may not adequately address the relationship between viral load in the brain and the observed neurobehavioral changes prior to death. Mechanisms of virus-induced alterations in neuronal function, either directly or indirectly, must be determined in order to target appropriate therapies to prevent or correct the neuronal dysfunction. Examples of research that would be an appropriate response to this Program Announcement include, but are not limited to: o research to determine methods to effectively quantitate viral load within the CNS during life; o research to correlate the quantity of virus within the CNS to neurobehavioral changes; o research to identify specific alterations in the structure or function of neurons as a consequence of the presence of virus either directly or indirectly; o research that links HIV-induced altered neuronal structure or function to impaired motor/cognitive function; o research that links HIV-induced altered CNS physiology to motor/cognitive dysfunction; o research to identify and test drugs that prevent or reverse the altered CNS physiology or the associated motor/cognitive dysfunction; o research using any appropriate animal model that will allow the identification of the mechanisms underlying HIV- induced CNS dysfunction. Understanding the effects of HIV infection on the CNS will allow the identification of therapeutic intervention to either reverse or prevent this devastating complication of HIV. INCLUSION OF WOMEN AND MINORITIES IN RESEARCH INVOLVING HUMAN SUBJECTS It is the policy of the NIH that women and members of minority groups and their subpopulations must be included in all NIH supported biomedical and behavioral research projects involving human subjects, unless a clear and compelling rationale and justification is provided that inclusion is inappropriate with respect to the health of the subjects or the purpose of the research. This new policy results from the NIH Revitalization Act of 1993 (Section 492B of Public Law 103-43) and supersedes and strengthens the previous policies (Concerning the Inclusion of Women in Study Populations, and Concerning the Inclusion of Minorities in Study Populations), which have been in effect since 1990. The new policy contains some provisions that are substantially different from the 1990 policies. All investigators proposing research involving human subjects should read the "NIH Guidelines For Inclusion of Women and Minorities as Subjects in Clinical Research," which have been published in the Federal Register of March 28, 1994 (FR 59 14508-14513) and reprinted in the NIH Guide for Grants and Contracts, Volume 23, Number 11, March 18, 1994. Investigators also may obtain copies of the policy from the program staff listed under INQUIRIES. Program staff may also provide additional relevant information concerning the policy. APPLICATION PROCEDURES Applications (with the exception of F30, F31, F32) are to be submitted on the grant application form PHS 398 (rev. 5/95) and will be accepted at standard deadlines for AIDS applications as indicated on page 21 of the application kit. Applications for fellowships (F- Series) are to be submitted on form PHS 416-1 (rev. 8/95); the standard receipt dates for these applications are April 5, August 5, and December 5. Both application kits are available at most institutional offices of sponsored research and may be obtained from Office of Extramural Outreach and Information Resources, 6701 Rockledge Drive, MSC 7910, Bethesda, MD 20892-7910; telephone 301/710-0267; fax 301/480-0525; email: ASKNIH@ODROCKM1.OD.NIH.GOV. The title, "HIV: Viral Load in Brain and Neurobehavioral Correlates," and number of the program announcement must be typed on the face page of the application. Applications for the FIRST award (R29) must include at least three sealed reference letters attached to the face page of the original application. FIRST award (R29) applications submitted without the required number of reference letters will be considered incomplete and will be returned without review. Applications for individual NRSAs (F30, 31, 32) must submit at least three completed reference forms. These forms are enclosed in the PHS 416-1 (rev. 8/95) kit used for individual NRSA applications. The completed original application and five legible copies of the PHS 398 or the original and two copies of the PHS 416-1 must be sent or delivered to: DIVISION OF RESEARCH GRANTS NATIONAL INSTITUTES OF HEALTH 6701 ROCKLEDGE DRIVE, ROOM 1040 - MSC 7710 BETHESDA, MD 20892-7710 BETHESDA, MD 20817 (for courier/overnight mail service) REVIEW CONSIDERATIONS Applications will be assigned on the basis of established PHS referral guidelines. Applications that are complete will be evaluated for scientific and technical merit by an appropriate peer review group convened in accordance with the standard NIH peer review procedures. As part of the initial merit review, applications may receive a written critique and undergo a process in which only those applications deemed to have the highest scientific merit, generally the top half of applications under review, will be discussed, assigned a priority score, and receive a second level review by the appropriate national advisory council or board, when applicable. Review Criteria for R01 and R29 o scientific, technical, or medical significance and originality of proposed research; o appropriateness and adequacy of the experimental approach and methodology proposed to carry out the research; o qualifications and research experience of the Principal Investigator and staff, particularly, but not exclusively, in the area of the proposed research; o availability of the resources necessary to perform the research; o appropriateness of the proposed budget and duration in relation to the proposed research; o adequacy of plans to include both genders and minorities and their subgroups as appropriate for the scientific goals of the research. Plans for the recruitment and retention of subjects will also be evaluated. The initial review group will also examine the provisions for the protection of human and animal subjects, the safety of the research environment, and conformance with the NIH Guidelines for the Inclusion of Women and Minorities as Subjects in Clinical Research. AWARD CRITERIA Applications will compete for available funds with all other approved applications. The following will be considered in making funding decisions: quality of the proposed project as determined by peer review availability of funds, and program priority. INQUIRIES Inquiries regarding this PA are encouraged. The opportunity to clarify any issues or questions from potential applicants is welcome. Direct inquiries regarding programmatic issues relating to the neurobehavioral impairments associated with HIV infection to: Dianne M. Rausch, Ph.D. Office on AIDS National Institute of Mental Health Parklawn Building, Room 10-75 Bethesda, MD 20857 Telephone: (301) 443-6100 FAX: (301) 443-7274 Email: dr89b@nih.gov Direct inquiries regarding programmatic issues relating to the neurological complications of HIV infection to: A. P. Kerza-Kwiatecki, Ph.D. Division of Demyelinating, Atrophic, and Dementing Disorders National Institute of Neurological Disorders and Stroke Federal Building, Room 804 7550 Wisconsin Avenue Bethesda, MD 20892 Telephone: (301) 496-1431 FAX: (301) 402-2060 Email: ak45w@nih.gov Direct inquiries regarding fiscal matters to: Diana S. Trunnell Grants Management Branch National Institute of Mental Health Parklawn Building, Room 7C-08 Bethesda, MD 20857 Telephone: (301) 443-3065 FAX: (301) 443-6885 Email: Diana_Trunnell@nih.gov Dianna Jessee Division of Extramural Activities National Institute of Neurological Disorders and Stroke Federal Building, Room 1004 7550 Wisconsin Avenue Bethesda, MD 20892 Telephone: (301) 496-9231 FAX: (301) 402-0219 Email: dj35j@nih.gov AUTHORITY AND REGULATIONS This program is described in the Catalog of Federal Domestic Assistance Nos. 93.242, 93.281, and 93.282 for NIMH, and Nos. 93.853 and 93.854 for NINDS. Awards are made under authorization of the Public Health Service Act, Title IV, Part A (Public Law 78-410, as amended by Public Law 99-158, 42 USC 241 and 285) and administered under PHS grants policies and Federal Regulations 42 CFR 52 and 66, and 45 CFR Part 74. This program is not subject to the intergovernmental review requirements of Executive Order 12372 or Health Systems Agency review. Awards will be administered under PHS grants policy as stated in the Public Health Service Grants Policy Statement (April 1, 1994). The PHS strongly encourages all grant and contract recipients to provide a smoke-free workplace and promote the nonuse of all tobacco products. In addition, Public Law 103-227, the Pro- Children Act of 1994, prohibits smoking in certain facilities (or in some cases, any portion of a facility) in which regular or routine education, library, day care, health care or early childhood development services are provided to children. This is consistent with the PHS mission to protect and advance the physical and mental health of the American people. .
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