review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Sergey Yegorov | Q37375503 |
P2093 | author name string | Rupert Kaul | |
Sara V Good | |||
Ronald M Galiwango | |||
Vineet Joag | |||
Brenda Okech | |||
P2860 | cites work | Examining the relationship between urogenital schistosomiasis and HIV infection | Q24290707 |
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Integrin ligands at a glance | Q24600618 | ||
Helminth infections: the great neglected tropical diseases | Q24648324 | ||
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"Rapid-impact interventions": how a policy of integrated control for Africa's neglected tropical diseases could benefit the poor | Q24810845 | ||
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Impact of human schistosomiasis in sub-Saharan Africa | Q26825064 | ||
Regulation of type I interferon responses | Q26853177 | ||
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CD4+CD25+ regulatory cells contribute to the regulation of colonic Th2 granulomatous pathology caused by schistosome infection | Q27306067 | ||
Vaginal challenge with an SIV-based dual reporter system reveals that infection can occur throughout the upper and lower female reproductive tract | Q27323310 | ||
S. mansoni bolsters anti-viral immunity in the murine respiratory tract | Q27329934 | ||
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Immune activation is a dominant factor in the pathogenesis of African AIDS | Q28300684 | ||
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Heterosexual risk of HIV-1 infection per sexual act: systematic review and meta-analysis of observational studies | Q28307869 | ||
IFN-λ4 Attenuates Antiviral Responses by Enhancing Negative Regulation of IFN Signaling. | Q47600393 | ||
Evaluation of the association between the concentrations of key vaginal bacteria and the increased risk of HIV acquisition in African women from five cohorts: a nested case-control study. | Q50066790 | ||
Vaginal microbiota and susceptibility to HIV. | Q50101300 | ||
αEβ7, α4β7 and α4β1 integrin contributions to T cell distribution in blood, cervix and rectal tissues: Potential implications for HIV transmission | Q50114397 | ||
The Human Penis Is a Genuine Immunological Effector Site | Q50130439 | ||
Decreased Sensitivity of Schistosoma sp. Egg Microscopy in Women and HIV-Infected Individuals | Q50192319 | ||
Immunological profile of heterosexual highly HIV-exposed uninfected individuals: predominant role of CD4 and CD8 T-cell activation. | Q51970423 | ||
Decreased CD4 and increased CD8 counts with T cell activation is associated with chronic helminth infection. | Q52036421 | ||
Adhesion and co-stimulatory molecules in the pathogenesis of hepatic and intestinal schistosomiasis mansoni. | Q52185190 | ||
Broadly neutralizing antibodies for treatment and prevention of HIV-1 infection. | Q52561746 | ||
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The Role of Integrin α4β7 in HIV Pathogenesis and Treatment. | Q52686548 | ||
Gene expression profile of CD4+ T cells reveals an interferon signaling suppression associated with progression of experimental Schistosoma japonicum infection | Q53914245 | ||
"Rapid impact" 10 years after: The first "decade" (2006-2016) of integrated neglected tropical disease control. | Q55103665 | ||
Ex vivo HIV entry into blood CD4+ T cells does not predict heterosexual HIV acquisition in women | Q56930898 | ||
Sexual Transmission and Propagation of SIV and HIV in Resting and Activated CD4+ T Cells | Q57075707 | ||
IL-15 regulates susceptibility of CD4 T cells to HIV infection | Q57292232 | ||
Interleukin-15-Stimulated Natural Killer Cells Clear HIV-1-Infected Cells following Latency Reversal | Q57425155 | ||
Gene Expression Differences in Host Response to Schistosoma haematobium Infection. | Q57463003 | ||
Double-stranded RNAs from the Helminth ParasiteSchistosomaActivate TLR3 in Dendritic Cells | Q57518104 | ||
A distinct cytokine and chemokine profile at the genital mucosa is associated with HIV-1 protection among HIV-exposed seronegative commercial sex workers | Q57766050 | ||
Dynamic changes in human-gut microbiome in relation to a placebo-controlled anthelminthic trial in Indonesia | Q57929815 | ||
High levels of TNF, soluble TNF receptors, soluble ICAM-1, and IFN-gamma, but low levels of IL-5, are associated with hepatosplenic disease in human schistosomiasis mansoni | Q58312856 | ||
Prevalence of urinary schistosomiasis and HIV in females living in a rural community of Zimbabwe: does age matter? | Q58380016 | ||
IL-15 enhances survival and function of HIV-specific CD8+ T cells | Q58479905 | ||
Schistosoma mansoni infection and socio-behavioural predictors of HIV risk: a cross-sectional study in women from Uganda | Q59330001 | ||
Schistosomiasis is associated with incident HIV transmission and death in Zambia | Q60302533 | ||
Urogenital schistosomiasis is associated with signatures of microbiome dysbiosis in Nigerian adolescents | Q61443105 | ||
Alterations of the Mice Gut Microbiome via Ova-Induced Granuloma | Q64062438 | ||
Reported oral and anal sex among adolescents and adults reporting heterosexual sex in sub-Saharan Africa: a systematic review | Q64066102 | ||
Female genital schistosomiasis and HIV/AIDS: Reversing the neglect of girls and women | Q64077656 | ||
The Impact of Anthelmintic Treatment on Human Gut Microbiota Based on Cross-Sectional and Pre- and Postdeworming Comparisons in Western Kenya | Q64097401 | ||
Schistosoma mansoni treatment reduces HIV entry into cervical CD4+ T cells and induces IFN-I pathways | Q64283612 | ||
Defining early SIV replication and dissemination dynamics following vaginal transmission | Q64290549 | ||
Immune attrition of adult schistosomes | Q72834060 | ||
II. The distribution of schistosome ova in the genito-urinary tract in subjects of bilharziasis | Q73230102 | ||
Changes to the cytokine microenvironment in the genital tract mucosa of HIV+ women | Q74497755 | ||
Genital manifestations of schistosomiasis mansoni in women: important but neglected | Q77913872 | ||
Low-level CD4+ T cell activation is associated with low susceptibility to HIV-1 infection | Q81375635 | ||
Altered Cervical Mucosal Gene Expression and Lower Interleukin 15 Levels in Women With Schistosoma haematobium Infection but Not in Women With Schistosoma mansoni Infection | Q90780437 | ||
Characterization of CD4+ T cell subsets and HIV susceptibility in the inner and outer foreskin of Ugandan men | Q91972771 | ||
Wuchereria bancrofti infection is linked to systemic activation of CD4 and CD8 T cells | Q92697462 | ||
Interactions between Parasitic Infections and the Human Gut Microbiome in Odisha, India | Q92964163 | ||
CD4+CD25hiFOXP3+ Regulatory T Cells and Cytokine Responses in Human Schistosomiasis before and after Treatment with Praziquantel | Q35751348 | ||
Schistosoma mansoni Infection in Ugandan Men Is Associated with Increased Abundance and Function of HIV Target Cells in Blood, but Not the Foreskin: A Cross-sectional Study | Q35763313 | ||
Foreskin T-cell subsets differ substantially from blood with respect to HIV co-receptor expression, inflammatory profile, and memory status | Q35782953 | ||
Immune Activation in the Female Genital Tract: Expression Profiles of Soluble Proteins in Women at High Risk for HIV Infection | Q35905458 | ||
Variable effect of co-infection on the HIV infectivity: within-host dynamics and epidemiological significance | Q35914310 | ||
Schistosoma mansoni and HIV acquisition in fishing communities of Lake Victoria, Uganda: a nested case-control study | Q35929451 | ||
Genital inflammation and the risk of HIV acquisition in women | Q36049017 | ||
Schistosoma mansoni and HIV infection in a Ugandan population with high HIV and helminth prevalence | Q36055791 | ||
Understanding the gender disparity in HIV infection across countries in sub-Saharan Africa: evidence from the Demographic and Health Surveys | Q36141387 | ||
Unique features of antiviral immune system of the vaginal mucosa | Q36177229 | ||
Downregulation of Th1 cytokine production accompanies induction of Th2 responses by a parasitic helminth, Schistosoma mansoni | Q36229789 | ||
Perils at mucosal front lines for HIV and SIV and their hosts | Q36274922 | ||
Increased density of human immunodeficiency virus type 1 coreceptors CCR5 and CXCR4 on the surfaces of CD4(+) T cells and monocytes of patients with Schistosoma mansoni infection | Q36375958 | ||
Innate immune activation enhances hiv acquisition in women, diminishing the effectiveness of tenofovir microbicide gel. | Q36410030 | ||
Focusing the HIV response through estimating the major modes of HIV transmission: a multi-country analysis | Q36440480 | ||
Association of Schistosomiasis and HIV infection in Tanzania | Q36450647 | ||
Protective immune mechanisms in helminth infection | Q36481763 | ||
Mast cells and histamine alter intestinal permeability during malaria parasite infection | Q36494811 | ||
Increased adhesion of Plasmodium falciparum infected erythrocytes to ICAM-1 in children with acute intestinal injury | Q36529834 | ||
T-helper 17 cells are associated with pathology in human schistosomiasis | Q36606601 | ||
HIV and Schistosoma haematobium prevalences correlate in sub-Saharan Africa | Q36701899 | ||
Th17 Cells Are Preferentially Infected Very Early after Vaginal Transmission of SIV in Macaques | Q36826452 | ||
Rapid Inflammasome Activation following Mucosal SIV Infection of Rhesus Monkeys | Q36828434 | ||
Association Between Schistosoma haematobium Exposure and Human Immunodeficiency Virus Infection Among Females in Mozambique | Q36869515 | ||
Regulatory T-Cell Activity But Not Conventional HIV-Specific T-Cell Responses Are Associated With Protection From HIV-1 Infection | Q36900870 | ||
Induction and regulation of pathogenic Th17 cell responses in schistosomiasis | Q36949600 | ||
Setting the stage: host invasion by HIV. | Q36983857 | ||
Effect of helminth-induced immunity on infections with microbial pathogens | Q37113913 | ||
Prevention of SHIV transmission by topical IFN-β treatment | Q37150111 | ||
Defining the interaction of HIV-1 with the mucosal barriers of the female reproductive tract | Q37252653 | ||
Preferential HIV infection of CCR6+ Th17 cells is associated with higher levels of virus receptor expression and lack of CCR5 ligands | Q37252952 | ||
Malaria-associated L-arginine deficiency induces mast cell-associated disruption to intestinal barrier defenses against nontyphoidal Salmonella bacteremia | Q37264637 | ||
Virologic and immunologic determinants of heterosexual transmission of human immunodeficiency virus type 1 in Africa. | Q37357668 | ||
Increased gastrointestinal permeability in patients with Plasmodium falciparum malaria. | Q39592902 | ||
Dynamics of CCR5 expression by CD4(+) T cells in lymphoid tissues during simian immunodeficiency virus infection | Q39597678 | ||
The future of mucosal immunology: studying an integrated system-wide organ | Q39862049 | ||
Resistance to Simian HIV infection is associated with high plasma interleukin-8, RANTES and Eotaxin in a macaque model of repeated virus challenges | Q39899694 | ||
Preventing HIV infection without targeting the virus: how reducing HIV target cells at the genital tract is a new approach to HIV prevention | Q40047164 | ||
The biology of how circumcision reduces HIV susceptibility: broader implications for the prevention field | Q40047225 | ||
Effect of HSV-2 infection on subsequent HIV acquisition: an updated systematic review and meta-analysis | Q40069410 | ||
Vaginal bacteria modify HIV tenofovir microbicide efficacy in African women | Q40176907 | ||
Schistosomiasis and Human Immunodeficiency Virus in Men in Tanzania | Q40342637 | ||
A type I IFN-dependent pathway induced by Schistosoma mansoni eggs in mouse myeloid dendritic cells generates an inflammatory signature | Q40587016 | ||
A TH1-->TH2 switch is a critical step in the etiology of HIV infection | Q40709038 | ||
Increased levels of inflammatory cytokines in the female reproductive tract are associated with altered expression of proteases, mucosal barrier proteins, and an influx of HIV-susceptible target cells | Q40805771 | ||
Intranasal immunization with CpG oligodeoxynucleotides as an adjuvant dramatically increases IgA and protection against herpes simplex virus-2 in the genital tract | Q40826626 | ||
Host parasite communications-Messages from helminths for the immune system: Parasite communication and cell-cell interactions | Q40997286 | ||
Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1. | Q41541656 | ||
A common mucosal immunologic system involving the bronchus, breast and bowel | Q41808590 | ||
Effects of schistosomiasis on susceptibility to HIV-1 infection and HIV-1 viral load at HIV-1 seroconversion: A nested case-control study. | Q41930746 | ||
CD4 T cells with effector memory phenotype and function develop in the sterile environment of the fetus | Q42213414 | ||
The HIV-1 transmission bottleneck | Q42314454 | ||
Pathways to increased coverage: an analysis of time trends in contraceptive need and use among adolescents and young women in Kenya, Rwanda, Tanzania, and Uganda | Q42682496 | ||
Decreased immune activation in resistance to HIV-1 infection is associated with an elevated frequency of CD4(+)CD25(+)FOXP3(+) regulatory T cells | Q43468180 | ||
A Quantitative Post-Mortem Study of Schistosomiasis Mansoni in Man | Q43486155 | ||
Schistosoma mansoni and S. haematobium infections in Egypt. III. Extrahepatic pathology. | Q43576817 | ||
Increased CCR5 and CXCR4 expression in Ethiopians living in Israel: environmental and constitutive factors | Q43646257 | ||
Cross-sectional relationship between HIV, lymphatic filariasis and other parasitic infections in adults in coastal northeastern Tanzania | Q43947376 | ||
Female genital schistosomiasis of the lower genital tract: prevalence and disease-associated morbidity in northern Tanzania | Q43951838 | ||
Impact of microscopy error on estimates of protective efficacy in malaria-prevention trials | Q44113989 | ||
Multispecies schistosomal infections of the female genital tract detected in cytology smears | Q44158314 | ||
Levels of innate immune factors in genital fluids: association of alpha defensins and LL-37 with genital infections and increased HIV acquisition | Q44560361 | ||
Association between acquisition of herpes simplex virus type 2 in women and bacterial vaginosis | Q45722454 | ||
Mucosal and systemic immune activation is present in human immunodeficiency virus-exposed seronegative women | Q45740268 | ||
Vaginal lactobacilli, microbial flora, and risk of human immunodeficiency virus type 1 and sexually transmitted disease acquisition | Q45746359 | ||
Plasmodium falciparum antigen-induced human immunodeficiency virus type 1 replication is mediated through induction of tumor necrosis factor-alpha | Q45757919 | ||
Inhibiting the Ins and Outs of HIV Replication: Cell-Intrinsic Antiretroviral Restrictions at the Plasma Membrane | Q47550785 | ||
Potential cost-effectiveness of schistosomiasis treatment for reducing HIV transmission in Africa--the case of Zimbabwean women | Q28535033 | ||
Differences in the Faecal Microbiome in Schistosoma haematobium Infected Children vs. Uninfected Children | Q28545859 | ||
Human Immunodeficiency Virus, Antiretroviral Therapy and Markers of Lymphatic Filariasis Infection: A Cross-sectional Study in Rural Northern Malawi | Q28547873 | ||
Prevalence of Lymphatic Filariasis and Treatment Effectiveness of Albendazole/ Ivermectin in Individuals with HIV Co-infection in Southwest-Tanzania | Q28551292 | ||
P. falciparum enhances HIV replication in an experimental malaria challenge system | Q28727971 | ||
Viral load and heterosexual transmission of human immunodeficiency virus type 1. Rakai Project Study Group | Q29614934 | ||
Human schistosomiasis | Q29619142 | ||
Antiretroviral preexposure prophylaxis for heterosexual HIV transmission in Botswana | Q29620078 | ||
Schistosomiasis is more prevalent than previously thought: what does it mean for public health goals, policies, strategies, guidelines and intervention programs? | Q30235149 | ||
Propagation and dissemination of infection after vaginal transmission of simian immunodeficiency virus | Q30350983 | ||
Women and HIV in Sub-Saharan Africa. | Q30356708 | ||
Targeting early infection to prevent HIV-1 mucosal transmission. | Q30386549 | ||
Early Events in Sexual Transmission of HIV and SIV and Opportunities for Interventions | Q30395919 | ||
Characterization of a human cervical CD4+ T cell subset coexpressing multiple markers of HIV susceptibility | Q30408905 | ||
Quality and quantity: mucosal CD4+ T cells and HIV susceptibility | Q30412727 | ||
Hormonal contraceptive use and women's risk of HIV acquisition: a meta-analysis of observational studies | Q30660068 | ||
Acute Schistosoma mansoni infection increases susceptibility to systemic SHIV clade C infection in rhesus macaques after mucosal virus exposure | Q33354076 | ||
Detectable urogenital schistosome DNA and cervical abnormalities 6 months after single-dose praziquantel in women with Schistosoma haematobium infection | Q33582198 | ||
The rectal mucosa and condomless receptive anal intercourse in HIV-negative MSM: implications for HIV transmission and prevention | Q33694217 | ||
Effect of female genital schistosomiasis and anti-schistosomal treatment on monocytes, CD4+ T-cells and CCR5 expression in the female genital tract | Q33711969 | ||
HIV infection and immune defense of the penis | Q33788345 | ||
Simian immunodeficiency virus rapidly penetrates the cervicovaginal mucosa after intravaginal inoculation and infects intraepithelial dendritic cells | Q33806915 | ||
Intravaginal practices, bacterial vaginosis, and HIV infection in women: individual participant data meta-analysis | Q33831737 | ||
Protection against genital herpes infection in mice immunized under different hormonal conditions correlates with induction of vagina-associated lymphoid tissue | Q33835473 | ||
Evolution of Th2 immunity: a rapid repair response to tissue destructive pathogens. | Q33904042 | ||
Schistosoma mansoni enhances host susceptibility to mucosal but not intravenous challenge by R5 Clade C SHIV | Q33988944 | ||
No evidence of association between HIV-1 and malaria in populations with low HIV-1 prevalence | Q33999657 | ||
Good cell, bad cell: flow cytometry reveals T-cell subsets important in HIV disease | Q34007172 | ||
Determinants of per-coital-act HIV-1 infectivity among African HIV-1-serodiscordant couples | Q34030252 | ||
HIV transmission risk through anal intercourse: systematic review, meta-analysis and implications for HIV prevention | Q34088757 | ||
Phenotype and susceptibility to HIV infection of CD4+ Th17 cells in the human female reproductive tract | Q34381171 | ||
Blunted IL17/IL22 and pro-inflammatory cytokine responses in the genital tract and blood of HIV-exposed, seronegative female sex workers in Kenya | Q34395906 | ||
Mucosal immunity and vaccines | Q34409172 | ||
Increased prevalence of leukocytes and elevated cytokine levels in semen from Schistosoma haematobium-infected individuals. | Q34412395 | ||
Human schistosomiasis | Q34413522 | ||
Coinfection. Virus-helminth coinfection reveals a microbiota-independent mechanism of immunomodulation | Q35216939 | ||
Cross-Sectional Analysis of Selected Genital Tract Immunological Markers and Molecular Vaginal Microbiota in Sub-Saharan African Women, with Relevance to HIV Risk and Prevention | Q35548029 | ||
Type I interferon responses in rhesus macaques prevent SIV infection and slow disease progression | Q35564886 | ||
Cervicovaginal bacteria are a major modulator of host inflammatory responses in the female genital tract | Q35636288 | ||
Plasma cytokine levels and risk of HIV type 1 (HIV-1) transmission and acquisition: a nested case-control study among HIV-1-serodiscordant couples | Q35661895 | ||
HIV and mucosal barrier interactions: consequences for transmission and pathogenesis | Q35685260 | ||
Schistosomiasis japonica during pregnancy is associated with elevated endotoxin levels in maternal and placental compartments | Q37443051 | ||
Resistance to type 1 interferons is a major determinant of HIV-1 transmission fitness | Q37612507 | ||
Real-time polymerase chain reaction for detection of Schistosoma DNA in small-volume urine samples reflects focal distribution of urogenital Schistosomiasis in primary school girls in KwaZulu Natal, South Africa | Q37623303 | ||
Genital-Systemic Chemokine Gradients and the Risk of HIV Acquisition in Women | Q37639078 | ||
HIV Infection in Uncircumcised Men Is Associated With Altered CD8 T-cell Function But Normal CD4 T-cell Numbers in the Foreskin | Q37671931 | ||
The Envelope Gene of Transmitted HIV-1 Resists a Late Interferon Gamma-Induced Block. | Q37707466 | ||
Immune correlates of HIV exposure without infection in foreskins of men from Rakai, Uganda | Q37720097 | ||
Chemoattractant-mediated leukocyte trafficking enables HIV dissemination from the genital mucosa | Q37730789 | ||
Defining genital tract cytokine signatures of sexually transmitted infections and bacterial vaginosis in women at high risk of HIV infection: a cross-sectional study | Q37843826 | ||
Defining the human T helper 17 cell phenotype. | Q38017373 | ||
Human Th17 subsets | Q38040742 | ||
Considering treatment of male genital schistosomiasis as a tool for future HIV prevention: a systematic review | Q38571811 | ||
Type I interferon is required for T helper (Th) 2 induction by dendritic cells | Q38674915 | ||
Regulation of the host immune system by helminth parasites | Q38835948 | ||
Periportal fibrosis in human Schistosoma mansoni infection is associated with low IL-10, low IFN-gamma, high TNF-alpha, or low RANTES, depending on age and gender | Q38882456 | ||
Probability of HIV-1 transmission per coital act in monogamous, heterosexual, HIV-1-discordant couples in Rakai, Uganda | Q38885289 | ||
Female genital schistosomiasis as a risk-factor for the transmission of HIV. | Q38889336 | ||
Murine Plasmodium chabaudi malaria increases mucosal immune activation and the expression of putative HIV susceptibility markers in the gut and genital mucosae | Q38940970 | ||
HIV-malaria co-infection: effects of malaria on the prevalence of HIV in East sub-Saharan Africa | Q38957309 | ||
Enteric helminth-induced type I interferon signaling protects against pulmonary virus infection through interaction with the microbiota. | Q38961697 | ||
The pathology of schistosomiasis in Ibadan, Nigeria with special reference to the appendix, brain, pancreas and genital organs | Q38982265 | ||
Lactobacillus-Deficient Cervicovaginal Bacterial Communities Are Associated with Increased HIV Acquisition in Young South African Women | Q39021401 | ||
Why do young women have a much higher prevalence of HIV than young men? A study in Kisumu, Kenya and Ndola, Zambia | Q39025507 | ||
Filarial infections increase susceptibility to human immunodeficiency virus infection in peripheral blood mononuclear cells in vitro | Q39028977 | ||
Identification of preferential CD4+ T-cell targets for HIV infection in the cervix. | Q39108028 | ||
Simple clinical manifestations of genital Schistosoma haematobium infection in rural Zimbabwean women | Q39140070 | ||
Effect of Wuchereria bancrofti infection on HIV incidence in southwest Tanzania: a prospective cohort study | Q39148927 | ||
Contribution of type III interferons to antiviral immunity: location, location, location | Q39176570 | ||
Confidential HIV testing and condom promotion in Africa. Impact on HIV and gonorrhea rates | Q39232951 | ||
Progesterone-based compounds affect immune responses and susceptibility to infections at diverse mucosal sites | Q39237289 | ||
CD69: from activation marker to metabolic gatekeeper. | Q39285769 | ||
A quantitative post mortem analysis of urinary schistosomiasis in Egypt. II. Evolution and epidemiology | Q39472521 | ||
A systematic review of the epidemiologic interactions between classic sexually transmitted diseases and HIV: how much really is known? | Q34426356 | ||
Reduced cellular susceptibility to in vitro HIV infection is associated with CD4+ T cell quiescence | Q34430345 | ||
Evidence of microbial translocation associated with perturbations in T cell and antigen-presenting cell homeostasis in hookworm infections | Q34443099 | ||
HIV-1 and interferons: who's interfering with whom? | Q34473801 | ||
Human schistosomiasis is associated with endotoxemia and Toll-like receptor 2- and 4-bearing B cells | Q34531341 | ||
Low prevalence of laboratory-confirmed malaria in clinically diagnosed adult women from the Wakiso district of Uganda | Q34544654 | ||
Potential HIV-1 target cells in the human penis | Q34548480 | ||
Ensuring quality and access for malaria diagnosis: how can it be achieved? | Q34557841 | ||
Impact of asymptomatic Herpes simplex virus-2 infection on T cell phenotype and function in the foreskin | Q34562540 | ||
Malaria biology and disease pathogenesis: insights for new treatments | Q34579700 | ||
Urogenital schistosomiasis in women of reproductive age in Tanzania's Lake Victoria region | Q34592127 | ||
Vaginal memory T cells induced by intranasal vaccination are critical for protective T cell recruitment and prevention of genital HSV-2 disease | Q34594102 | ||
Endotoxaemia is common in children with Plasmodium falciparum malaria | Q34622540 | ||
S. haematobium as a common cause of genital morbidity in girls: a cross-sectional study of children in South Africa | Q34654161 | ||
Maternal Schistosomiasis japonica is associated with maternal, placental, and fetal inflammation | Q34739827 | ||
Effect of treating co-infections on HIV-1 viral load: a systematic review | Q34767216 | ||
Rethinking the heterosexual infectivity of HIV-1: a systematic review and meta-analysis | Q34804928 | ||
Glycerol monolaurate prevents mucosal SIV transmission | Q34957016 | ||
Activated CD4+CCR5+ T cells in the rectum predict increased SIV acquisition in SIVGag/Tat-vaccinated rhesus macaques. | Q34985353 | ||
Selective transmission of R5 HIV-1 variants: where is the gatekeeper? | Q35018140 | ||
Evaluating the potential impact of mass praziquantel administration for HIV prevention in Schistosoma haematobium high-risk communities | Q35048242 | ||
Peripheral blood CCR4+CCR6+ and CXCR3+CCR6+CD4+ T cells are highly permissive to HIV-1 infection | Q35064033 | ||
Vaccines that stimulate T cell immunity to HIV-1: the next step | Q35073079 | ||
Foreskin surface area and HIV acquisition in Rakai, Uganda (size matters) | Q35076140 | ||
IL-4 suppresses the responses to TLR7 and TLR9 stimulation and increases the permissiveness to retroviral infection of murine conventional dendritic cells | Q35086719 | ||
High prevalence of liver fibrosis associated with HIV infection: a study in rural Rakai, Uganda | Q35125231 | ||
Helminths and HIV infection: epidemiological observations on immunological hypotheses | Q35131194 | ||
Helminth-associated systemic immune activation and HIV co-receptor expression: response to albendazole/praziquantel treatment | Q35133510 | ||
Retinoic acid as a vaccine adjuvant enhances CD8+ T cell response and mucosal protection from viral challenge | Q35140438 | ||
HIV-1 infection of human penile explant tissue and protection by candidate microbicides | Q35148241 | ||
Systemic impact of intestinal helminth infections | Q35148851 | ||
The role of coinfections in HIV epidemic trajectory and positive prevention: a systematic review and meta-analysis | Q35149893 | ||
Schistosoma haematobium infection and CD4+ T-cell levels: a cross-sectional study of young South African women | Q35175398 | ||
HIV-1 sexual transmission: early events of HIV-1 infection of human cervico-vaginal tissue in an optimized ex vivo model. | Q35215387 | ||
P921 | main subject | Sub-Saharan Africa | Q132959 |
P304 | page(s) | 22 | |
P577 | publication date | 2019-11-29 | |
P1433 | published in | Tropical diseases, travel medicine and vaccines | Q27727112 |
P1476 | title | Impact of Endemic Infections on HIV Susceptibility in Sub-Saharan Africa | |
P478 | volume | 5 |
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