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1.
PLoS One ; 12(7): e0180796, 2017.
Article in English | MEDLINE | ID: mdl-28686678

ABSTRACT

HIV rapid diagnostic tests (RDTs) combined in an algorithm are the current standard for HIV diagnosis in many sub-Saharan African countries, and extensive laboratory testing has confirmed HIV RDTs have excellent sensitivity and specificity. However, false-positive RDT algorithm results have been reported due to a variety of factors, such as suboptimal quality assurance procedures and inaccurate interpretation of results. We conducted HIV serosurveys in seven sub-Saharan African military populations and recorded the frequency of personnel self-reporting HIV positivity, but subsequently testing HIV-negative during the serosurvey. The frequency of individuals who reported they were HIV-positive but subsequently tested HIV-negative using RDT algorithms ranged from 3.3 to 91.1%, suggesting significant rates of prior false-positive HIV RDT algorithm results, which should be confirmed using biological testing across time in future studies. Simple measures could substantially reduce false-positive results, such as greater adherence to quality assurance guidelines and prevalence-specific HIV testing algorithms as described in the World Health Organization's HIV testing guidelines. Other measures to improve RDT algorithm specificity include classifying individuals with weakly positive test lines as HIV indeterminate and retesting. While expansion of HIV testing in resource-limited countries is critical to identifying HIV-infected individuals for appropriate care and treatment, careful attention to potential causes of false HIV-positive results are needed to prevent the significant medical, psychological, and fiscal costs resulting from individuals receiving a false-positive HIV diagnosis.


Subject(s)
Algorithms , Diagnostic Tests, Routine , HIV Infections/diagnosis , Military Personnel , Adolescent , Adult , Africa South of the Sahara/epidemiology , False Positive Reactions , Female , HIV Infections/epidemiology , HIV Infections/psychology , Humans , Male , Mass Screening/methods , Practice Guidelines as Topic , Prevalence , Quality Assurance, Health Care/organization & administration , Self Report , Sensitivity and Specificity , World Health Organization
2.
Curr HIV Res ; 15(2): 116-127, 2017.
Article in English | MEDLINE | ID: mdl-28176644

ABSTRACT

INTRODUCTION: While sexual and gender-based violence (SGBV) is recognized as an important factor driving the HIV epidemic in sub-Saharan Africa, attitudes toward and prevalence of SGBV within sub-Saharan African military populations are unknown. Data on SGBV were collected from military service members of nine sub-Saharan African militaries. Attitudes related to SGBV and characteristics of those who commit and experience SGBV are reported. METHODS: Data for 8815 service members (8165 men and 650 women) aged 18 years or older who voluntarily participated in the Seroprevalence and Behavioral Epidemiology Risk Surveys from 2009 to 2014 were included in this secondary data analysis. Data were collected on demographics, HIV prevalence, SGBV attitudes, and experiences. Descriptive and bivariate statistical analyses were performed. RESULTS: 5% of men and 9% of women reported experiencing SGBV, and 6% of men reported they had ever committed SGBV. Men and women who had experienced SGBV were significantly more likely to agree with negative gender attitudes toward SGBV, and the majority of those who reported experiencing SGBV reported that SGBV was committed by someone outside of the military. CONCLUSION: This is the first study to examine SGBV in sub-Saharan military populations during periods of limited conflict. It provides evidence that SGBV is experienced by both male and female service members at rates not typically found in previous research examining SGBV in other military populations. A better understanding of SGBV in sub-Saharan military service members is necessary to ensure appropriate services and interventions are part of the military infrastructure.


Subject(s)
Gender-Based Violence , HIV Infections/epidemiology , Military Personnel , Sex Offenses , Adolescent , Adult , Africa South of the Sahara , Female , Humans , Male , Middle Aged , Seroepidemiologic Studies , Young Adult
3.
Sex Transm Infect ; 91(8): 581-8, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26586849

ABSTRACT

OBJECTIVES: Sexually transmitted infection (STI) prevalence and risk behaviour may differ at different phases of deployment. We examined STI prevalence and sexual behaviour in the predeployment time period (12 months prior) among recently deployed shipboard US Navy and Marine Corps military personnel. METHODS: Data were collected from 1938 male and 515 female service members through an anonymous, self-completed survey assessing sexual behaviours and STI acquisition characteristics in the past 12 months. Cross-sectional sex-stratified descriptive statistics are reported. RESULTS: Overall, 67% (n=1262/1896) reported last sex with a military beneficiary (spouse, n=931, non-spouse service member, n=331). Among those with a sexual partner outside their primary partnership, 24% (n=90/373) reported using a condom the last time they had sex and 30% (n=72/243) reported their outside partner was a service member. In total, 90% (n=210/233) reported acquiring their most recent STI in the USA (88%, n=126/143 among those reporting ≥1 deployments and an STI ≥1 year ago) and a significantly higher proportion (p<0.01) of women than men acquired the STI from their regular partner (54% vs 21%) and/or a service member (50% vs 26%). CONCLUSIONS: Findings suggest a complex sexual network among service members and military beneficiaries. Findings may extend to other mobile civilian and military populations. Data suggest most STI transmission within the shipboard community may occur in local versus foreign ports but analyses from later time points in deployment are needed. These data may inform more effective STI prevention interventions.


Subject(s)
Condoms/statistics & numerical data , Military Personnel/psychology , Military Personnel/statistics & numerical data , Sexual Behavior/statistics & numerical data , Sexual Partners/psychology , Sexually Transmitted Diseases/epidemiology , Sexually Transmitted Diseases/prevention & control , Adult , Cross-Sectional Studies , Female , Health Knowledge, Attitudes, Practice , Humans , Male , Prevalence , Risk-Taking , Sexual Behavior/psychology , Sexually Transmitted Diseases/transmission , United States/epidemiology
4.
Proc Natl Acad Sci U S A ; 102(37): 13218-23, 2005 Sep 13.
Article in English | MEDLINE | ID: mdl-16131544

ABSTRACT

The herpesvirus entry mediator (HVEM), a member of the TNF receptor (TNFR) superfamily, can act as a molecular switch that modulates T cell activation by propagating positive signals from the TNF-related ligand LIGHT (TNFR superfamily 14), or inhibitory signals through the Ig superfamily member B and T lymphocyte attenuator (BTLA). Competitive binding analysis and mutagenesis reveals a unique BTLA binding site centered on a critical lysine residue in cysteine-rich domain 1 of HVEM. The BTLA binding site on HVEM overlaps with the binding site for the herpes simplex virus 1 envelope glycoprotein D, but is distinct from where LIGHT binds, yet glycoprotein D inhibits the binding of both ligands, potentially nullifying the pathway. The binding site on HVEM for BTLA is conserved in the orphan TNFR, UL144, present in human CMV. UL144 binds BTLA, but not LIGHT, and inhibits T cell proliferation, selectively mimicking the inhibitory cosignaling function of HVEM. The demonstration that distinct herpesviruses target the HVEM-BTLA cosignaling pathway suggests the importance of this pathway in regulating T cell activation during host defenses.


Subject(s)
Herpesviridae/immunology , Lymphocyte Activation/immunology , Receptors, Immunologic/metabolism , Receptors, Tumor Necrosis Factor/physiology , Receptors, Virus/physiology , T-Lymphocytes/virology , Base Sequence , Binding Sites , Binding, Competitive , Cytomegalovirus/immunology , Cytomegalovirus/physiology , Herpesviridae/physiology , Herpesvirus 1, Human/immunology , Herpesvirus 1, Human/physiology , Humans , Membrane Glycoproteins/metabolism , Membrane Proteins/metabolism , Molecular Sequence Data , Phylogeny , Receptors, Tumor Necrosis Factor/immunology , Receptors, Tumor Necrosis Factor/metabolism , Receptors, Tumor Necrosis Factor, Member 14 , Receptors, Virus/immunology , Receptors, Virus/metabolism , Signal Transduction , T-Lymphocytes/immunology , Tumor Necrosis Factor Ligand Superfamily Member 14 , Tumor Necrosis Factor-alpha/metabolism , Viral Envelope Proteins/metabolism , Viral Proteins/metabolism
5.
J Biol Chem ; 278(50): 50523-9, 2003 Dec 12.
Article in English | MEDLINE | ID: mdl-14517219

ABSTRACT

Lymphotoxin-beta receptor (LTbetaR) and CD40 are members of the tumor necrosis factor family of signaling receptors that regulate cell survival or death through activation of NF-kappaB. These receptors transmit signals through downstream adaptor proteins called tumor necrosis factor receptor-associated factors (TRAFs). In this study, the crystal structure of a region of the cytoplasmic domain of LTbetaR bound to TRAF3 has revealed an unexpected new recognition motif, 388IPEEGD393, for TRAF3 binding. Although this motif is distinct in sequence and structure from the PVQET motif in CD40 and PIQCT in the regulator TRAF-associated NF-kappaB activator (TANK), recognition is mediated in the same binding crevice on the surface of TRAF3. The results reveal structurally adaptive "hot spots" in the TRAF3-binding crevice that promote molecular interactions driving specific signaling after contact with LTbetaR, CD40, or the downstream regulator TANK.


Subject(s)
Adaptor Proteins, Signal Transducing , CD40 Antigens/biosynthesis , Receptors, Tumor Necrosis Factor/chemistry , Signal Transduction , Amino Acid Motifs , Amino Acid Sequence , CD40 Antigens/chemistry , Cell Line , Cell Survival , Crystallography, X-Ray , DNA, Complementary/metabolism , Electrons , Glutathione Transferase/metabolism , Humans , Lymphotoxin beta Receptor , Models, Molecular , Molecular Sequence Data , Mutagenesis, Site-Directed , Peptides/chemistry , Protein Binding , Protein Conformation , Protein Structure, Secondary , Protein Structure, Tertiary , Proteins/metabolism , Receptors, Tumor Necrosis Factor/metabolism , Recombinant Fusion Proteins/metabolism
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