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Institution

Southern Research Institute

NonprofitDurham, North Carolina, United States
About: Southern Research Institute is a nonprofit organization based out in Durham, North Carolina, United States. It is known for research contribution in the topics: Virus & In vivo. The organization has 1965 authors who have published 2588 publications receiving 83306 citations.
Topics: Virus, In vivo, Purine, Viral replication, Nucleoside


Papers
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Journal ArticleDOI
20 Oct 2000-Science
TL;DR: The protective efficacy of vaccine-elicited immune responses against a pathogenic SHIV-89.6P challenge in rhesus monkeys is reported, with no evidence of clinical disease or mortality after challenge.
Abstract: With accumulating evidence indicating the importance of cytotoxic T lymphocytes (CTLs) in containing human immunodeficiency virus-1 (HIV-1) replication in infected individuals, strategies are being pursued to elicit virus-specific CTLs with prototype HIV-1 vaccines. Here, we report the protective efficacy of vaccine-elicited immune responses against a pathogenic SHIV-89.6P challenge in rhesus monkeys. Immune responses were elicited by DNA vaccines expressing SIVmac239 Gag and HIV-1 89.6P Env, augmented by the administration of the purified fusion protein IL-2/Ig, consisting of interleukin-2 (IL-2) and the Fc portion of immunoglobulin G (IgG), or a plasmid encoding IL-2/Ig. After SHIV-89.6P infection, sham-vaccinated monkeys developed weak CTL responses, rapid loss of CD4+ T cells, no virus-specific CD4+ T cell responses, high setpoint viral loads, significant clinical disease progression, and death in half of the animals by day 140 after challenge. In contrast, all monkeys that received the DNA vaccines augmented with IL-2/Ig were infected, but demonstrated potent secondary CTL responses, stable CD4+ T cell counts, preserved virus-specific CD4+ T cell responses, low to undetectable setpoint viral loads, and no evidence of clinical disease or mortality by day 140 after challenge.

926 citations

Journal ArticleDOI
TL;DR: In this paper, the thermal conductivity, thermal expansion, Youngs Modulus, flexural strength, and brittle-plastic deformation transition temperature of ZrB2, HfC 0·98 and HfN 0·92 ceramics were determined.
Abstract: The thermal conductivity, thermal expansion, Youngs Modulus, flexural strength, and brittle–plastic deformation transition temperature were determined for HfB2, HfC0·98, HfC0·67, and HfN0·92 ceramics. The oxidation resistance of ceramics in the ZrB2–ZrC–SiC system was characterized as a function of composition and processing technique. The thermal conductivity of HfB2 exceeded that of the other materials by a factor of 5 at room temperature and by a factor of 2·5 at 820°C. The transition temperature of HfC exhibited a strong stoichiometry dependence, decreasing from 2200°C for HfC0·98 to 1100°C for HfC0·67 ceramics. The transition temperature of HfB2 was 1100°C. The ZrB2/ZrC/SiC ceramics were prepared from mixtures of Zr (or ZrC), SiB4, and C using displacement reactions. The ceramics with ZrB2 as a predominant phase had high oxidation resistance up to 1500°C compared to pure ZrB2 and ZrC ceramics. The ceramics with ZrB2/SiC molar ratio of 2 (25 vol% SiC), containing little or no ZrC, were the most oxidation resistant.

716 citations

Journal ArticleDOI
TL;DR: Microspheres containing a toxoid vaccine of staphylococcal enterotoxin B effectively delivered and released the vaccine in the gutassociated lymphoid tissue as determined by their ability to induce a disseminated mucosal IgA anti-toxin antibody response.

702 citations

Journal ArticleDOI
17 Jan 2002-Nature
TL;DR: Viral escape from CTL recognition may be a major limitation of the CTL-based AIDS vaccines that are likely to be administered to large human populations over the next several years.
Abstract: Potent virus-specific cytotoxic T lymphocyte (CTL) responses elicited by candidate AIDS vaccines have recently been shown to control viral replication and prevent clinical disease progression after pathogenic viral challenges in rhesus monkeys. Here we show that viral escape from CTL recognition can result in the eventual failure of this partial immune protection. Viral mutations that escape from CTL recognition have been previously described in humans infected with human immunodeficiency virus (HIV) and monkeys infected with simian immunodeficiency virus (SIV). In a cohort of rhesus monkeys that were vaccinated and subsequently infected with a pathogenic hybrid simian-human immunodeficiency virus (SHIV), the frequency of viral sequence mutations within CTL epitopes correlated with the level of viral replication. A single nucleotide mutation within an immunodominant Gag CTL epitope in an animal with undetectable plasma viral RNA resulted in viral escape from CTLs, a burst of viral replication, clinical disease progression, and death from AIDS-related complications. These data indicate that viral escape from CTL recognition may be a major limitation of the CTL-based AIDS vaccines that are likely to be administered to large human populations over the next several years.

702 citations

Journal ArticleDOI
TL;DR: Pearly mussel research has begun to benefit from and contribute to current ideas about suspension feeding, life-history theory, metapopulations, flow refuges, spatial patterning and its effects, and management of endangered species.
Abstract: Pearly mussels (Unionacea) are widespread, abundant, and important in freshwater ecosystems around the world. Catastrophic declines in pearly mussel populations in North America and other parts of the world have led to a flurry of research on mussel biology, ecology, and conservation. Recent research on mussel feeding, life history, spatial patterning, and declines has augmented, modified, or overturned long-held ideas about the ecology of these animals. Pearly mussel research has begun to benefit from and contribute to current ideas about suspension feeding, life-history theory, metapopulations, flow refuges, spatial patterning and its effects, and management of endangered species. At the same time, significant gaps in understanding and apparent paradoxes in pearly mussel ecology have been exposed. To conserve remaining mussel populations, scientists and managers must simultaneously and aggressively pursue both rigorous research and conservation actions.

614 citations


Authors

Showing all 1965 results

NameH-indexPapersCitations
Joseph Sodroski13854277070
Beatrice H. Hahn12945869206
George M. Shaw12236560727
Sanford J. Shattil9923930840
Richard W. Compans9152631576
Jiri Mestecky9046928553
Michael R. Boyd6723619818
Brian A. MacVicar6716616082
Michael F. Summers6619416676
Christian C. Naus6618814811
David C. Coleman6216122162
Wayne T. Swank6217911697
Joanne E. Murphy-Ullrich6113313660
Ge Sun6030814161
Nalin Rastogi6038216293
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20221
202155
202061
201950
201863
201762