7 results on '"Zhuang, Ke"'
Search Results
2. CD4 + T cell depletion does not affect the level of viremia in chronically SHIV SF162P3N -infected Chinese cynomolgus monkeys.
- Author
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Liu H, Liu JB, Meng FZ, Xu XQ, Wang Y, Xian QY, Zhou RH, Xiao QH, Huang ZX, Zhou L, Li JL, Li XD, Wang X, Ho WZ, and Zhuang K
- Subjects
- Animals, CD4 Lymphocyte Count, CD4-Positive T-Lymphocytes cytology, China, Cytokines biosynthesis, Cytokines blood, Disease Progression, Female, Lymphocyte Activation immunology, Macaca fascicularis, Macrophages immunology, Macrophages virology, Proof of Concept Study, Simian Acquired Immunodeficiency Syndrome immunology, Simian Acquired Immunodeficiency Syndrome virology, Viral Load, CD4-Positive T-Lymphocytes immunology, Lymphocyte Depletion, Simian Immunodeficiency Virus immunology, Viremia blood, Virus Replication immunology
- Abstract
Chronically SHIV
SF162P3N -infected cynomolgus monkeys were used to determine the effects of the antibody-mediated acute CD4+ T cell depletion on viral load as well as on the immunological factors associated with disease progression. Compared with the control animals, CD4+ T cell-depleted animals with SHIV infection showed (i) little alteration in plasma viral load over the period of 22 weeks after the depletion; (ii) increased CD4+ T cell proliferation and turnover of macrophages at the early phase of the depletion, but subsequent decline to the basal levels; and (iii) little impact on the expression of the inflammatory cytokines and CC chemokines associated with disease progression. These findings indicate that the antibody-mediated acute CD4+ T cell depletion had minimal impact on plasma viral load and disease progression in chronically SHIVSF162P3N -infected cynomolgus monkeys. Future investigations are necessary to identify the key factor(s) related to the immune activation and macrophage infection during the CD4 deletion in chronic viral infection., (Copyright © 2021 Elsevier Inc. All rights reserved.)- Published
- 2021
- Full Text
- View/download PDF
3. Establishment and characterization of HBV-associated B lymphocytes with an immortalization potential.
- Author
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Qi X, Gui X, and Zhuang K
- Subjects
- Adult, Aged, Aged, 80 and over, B-Lymphocytes virology, Case-Control Studies, Cell Culture Techniques, Cell Transformation, Viral, Cells, Cultured, China epidemiology, Clone Cells, Female, Hepatitis B transmission, Humans, Lymphoma, B-Cell virology, Male, Middle Aged, Prevalence, Retrospective Studies, Young Adult, B-Lymphocytes pathology, Hepatitis B epidemiology, Hepatitis B virus isolation & purification, Lymphoma, B-Cell complications
- Abstract
Emerging evidences indicate that hepatitis B virus (HBV) infection is associated with non-Hodgkin lymphoma (NHL), but the mechanisms of HBV-induction lymphomagenesis remain unclear. In this report, retrospective analysis of the prevalence of hepatitis B surface antigen (HBsAg) among NHL cases demonstrated significantly higher HBsAg carrier rate among B-cell NHL cases than controls (other cancers except primary liver cancer) (adjusted odds ratio, 1.56; 95% confidence interval, 1.13-2.16). Furthermore, cells with an immortalization potential existed in the peripheral blood of 4 patients with chronic HBV infection. Characterization of these cells showed their immunophenotypes similar to that of the majority of HBsAg-positive B-cell NHL patients. Immunoglobulin (Ig) gene rearrangements confirmed the clonal Ig gene rearrangements. Cytogenetic analysis revealed abnormal karyotypes of these cells with an immortalization potential. Compared with cells with an immortalization potential that we previously found in B-cell NHL patients by the same way, these cells showed many similar features. In conclusion, cells with an immortalization potential existed in the part of patients with chronic HBV infection before lymphoma development and showed some malignant features. They may be the cellular basis of HBV-associated lymphomagenesis., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2019
- Full Text
- View/download PDF
4. Acute infection of Chinese macaques by a CCR5-tropic SHIV carrying a primary HIV-1 subtype B' envelope.
- Author
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Wang H, Zhuang K, Liu L, Tang Z, Tang J, Tien P, Zhang L, and Chen Z
- Subjects
- Animals, Asia, Southeastern, CD4-Positive T-Lymphocytes immunology, China, Genetic Engineering, Humans, Intestine, Small immunology, Macaca, Recombination, Genetic, Viral Tropism, Virulence, Disease Models, Animal, HIV-1 genetics, Receptors, CCR5 physiology, Receptors, Virus physiology, Simian Acquired Immunodeficiency Syndrome virology, Simian Immunodeficiency Virus genetics, Simian Immunodeficiency Virus pathogenicity
- Abstract
The increasing prevalence of HIV-1 subtype B' in China and Southeast Asia calls for efforts to develop a relevant animal model to study viral transmission and pathogenesis. Because there are significant differences between subtype B' HIV-1 and other chimeric simian/human immunodeficiency viru (SHIVs) in the env gene, a novel SHIV, designated SHIV(B'WHU), was generated by replacing counterparts of SHIV(SF33) with tat/rev/vpu/env genes derived from a primary, CCR5-tropic, subtype B' HIV-1 strain of a Chinese patient. SHIV(B'WHU) was able to replicate in rhesus peripheral blood mononuclear cells and used CCR5 as its major coreceptor. Moreover, after serial passages in Chinese macaques, the in vivo infectivity of SHIV(B'WHU) was enhanced, yet no significant sequence changes were found in viral envelopes, and the virus did not change its CCR5-tropism. CD4(+) T-cell loss, however, was found in the intraepithelial lymphocytes of small intestines of infected macaques. Our findings have implications in understanding the early pathogenesis of SHIV(B'WHU) in Chinese macaques.
- Published
- 2010
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- View/download PDF
5. Genetic characterization of full-length HIV type 1 genomes from 3 infected paid blood donors in Henan, China.
- Author
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Liu L, Su B, Zhuang K, Tien P, Chen Z, and Zhang L
- Subjects
- Base Sequence, China, Humans, Molecular Sequence Data, Phylogeny, Sequence Homology, Blood Donors, Genome, Viral, HIV Infections virology, HIV-1 genetics, HIV-1 isolation & purification
- Published
- 2005
- Full Text
- View/download PDF
6. High prevalence of HIV infection among women and their children in Henan Province, China.
- Author
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Zhuang K, Gui X, Su B, Tien P, Chen Z, and Zhang L
- Subjects
- Adult, Child, China epidemiology, Female, HIV Infections prevention & control, HIV Infections transmission, Humans, Pregnancy, Prevalence, Risk Factors, Rural Population, HIV Infections epidemiology, HIV-1
- Published
- 2003
- Full Text
- View/download PDF
7. [A survey of children with HIV/AIDS in highly epidemic villages of AIDS].
- Author
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Zhuang K, Gui XE, Luo JL, Wang XR, Su B, and Zhang YX
- Subjects
- Acquired Immunodeficiency Syndrome diagnosis, Acquired Immunodeficiency Syndrome epidemiology, Adolescent, Adult, Antibodies, Viral blood, Child, Child, Preschool, China epidemiology, Female, Gene Products, gag genetics, HIV Antigens genetics, HIV Infections diagnosis, HIV Infections epidemiology, HIV-1 genetics, HIV-1 immunology, Humans, Infant, Male, Polymerase Chain Reaction, Prevalence, gag Gene Products, Human Immunodeficiency Virus, Acquired Immunodeficiency Syndrome transmission, HIV Infections transmission, Infectious Disease Transmission, Vertical, Viral Proteins
- Abstract
Objective: To estimate prevalence of HIV/AIDS among children and the transmission routes in a highly endemic villages of AIDS., Methods: Totally 208 high-risk women of child bearing age and 159 of their children aged 0 - 14 years were investigated. Their medical histories of blood donation or transfusion were collected, blood samples were taken and sera were separated for HIV test. Enzyme-linked immunosorbent assay (ELISA) and Western blot assay were performed for HIV antibody. The Nested-polymerase chain reaction (PCR) assay amplifying gag gene p17 was performed on samples of children aged less than 18 months., Results: Thirty-seven HIV infected cases were found among 159 children aged 0 - 14 years of whom 33 were infected by mother-to-child transmission (89.2%, 33/37), 3 by blood transfusion (8.1%, 3/37) and one by iatrogenic route (2.7%, 1/37). Sixty seven mothers who were seropositive for HIV and their 86 children who were born after 1992 were investigated, 33 cases of them were infected with HIV. The rate of vertical transmission was 38.4% (33/86). The HIV vertical transmission rate among mothers with AIDS (68.8%, 22/32) was significantly greater than that among mothers with asymptomatic HIV infection (20.4%, 11/54, P < 0.05). The number of children infected with HIV through vertical transmission increased from 1993 to 2001. Among 37 children infected with HIV, 12 cases developed AIDS and 4 of them died, of whom 2 cases died from tuberculosis. The morbidity of AIDS was 27.3% (9/33). Ninety three point nine percent (31/33) of infected mothers didn't know their HIV seropositive status before pregnancy and delivery. Of 8 pregnant women infected with HIV, one had aggravation of AIDS, 2 miscarried, 2 terminated their pregnancy and 3 continued their pregnancy., Conclusion: Mother-to-child transmission of HIV was the major route of HIV/AIDS transmission to the children. The main reason leading to HIV infection in children was the lack of prenatal HIV counseling and testing for the high-risk women of childbearing age and lake of interventions. The countermeasures must be taken to control the further transmission of AIDS in order to protect the health of women and children in the highly endemic areas of AIDS.
- Published
- 2003
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