Immune responses against a new HIV-1 p24-gp41/pCAGGS-IL-12 DNA vaccine in Balb/c mice

Autor: Roodbari, Fatemeh, Sabahi, Farzaneh, Sarbolouki, Mohamad Nabi, Barkhordari, Farzaneh, Adeli, Ahmad, Jamedar, Amel, Mahboudi, Fereidoun
Přispěvatelé: Department of Virology, Faculty of Medical Sciences, Tarbiat Modares University [Tehran], Department of Cellular and Molecular Biology, Faculty of Basic Sciences, University of Mazandaran, Institute of Biochemistry and Biophysics, Tehran University of Basic Sciences, Biotechnology Research Center, Institut Pasteur d'Iran, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Department of Microbiology and Virology, Faculty of Medicine, Mashad University of Medical Sciences, This work was supported by a grant from Pasteur Institute of Iran, The authors would like to acknowledge the contributions of Ms. Rozita Edalat and Dr. Abbas Jamali in this research.
Rok vydání: 2012
Předmět:
MESH: Interleukin-12/metabolism
viruses
HIV Core Protein p24
HIV Infections
MESH: AIDS Vaccines/immunology
MESH: Recombinant Fusion Proteins/genetics
Mice
Vaccines
DNA

DNA Vaccine
Dendrosome
MESH: Animals
MESH: Interferon-gamma/metabolism
MESH: Immunity
Humoral

MESH: Interleukin-4/blood
Cells
Cultured

AIDS Vaccines
Immunity
Cellular

Mice
Inbred BALB C

virus diseases
MESH: HIV Core Protein p24/immunology
p24
gp41
Interleukin-12
HIV Envelope Protein gp41
MESH: HIV Envelope Protein gp41/genetics
MESH: HIV Infections/prevention & control
MESH: HIV Core Protein p24/genetics
MESH: Recombinant Fusion Proteins/immunology
IL-12
MESH: Immunization
[SDV.IMM]Life Sciences [q-bio]/Immunology
Female
MESH: HIV-1/immunology
MESH: Vaccines
DNA/immunology

MESH: Cells
Cultured

MESH: HIV Envelope Protein gp41/immunology
Recombinant Fusion Proteins
MESH: Mice
Inbred BALB C

MESH: Immunity
Cellular

Interferon-gamma
MESH: Interleukin-12/genetics
Animals
Humans
MESH: Mice
MESH: Humans
Immunity
Humoral

Immunoglobulin G
HIV-1
Immunization
Interleukin-4
MESH: Immunoglobulin G/blood
MESH: Female
Zdroj: Iranian Journal of Immunology
Iranian Journal of Immunology, Shiraz Institute for Cancer Research, 2012, 9 (2), pp.86-97
ISSN: 1735-367X
1735-1383
Popis: International audience; Background: Development of an effective vaccine is highly needed in order to restrict the AIDS pandemic. DNA vaccines initiate both arms of immunity without the potential of causing disease. HIV-1 p24 and gp41 (gag and env) proteins play important roles in viral pathogenesis and are effective candidates for immune induction and vaccine design. Objective: In this study, new DNA vaccine candidates constructed from HIV-1 fused p24-gp41 or gp41 alone were evaluated in Balb/c mice for induction of cellular and humoral immune responses. Methods: Recombinant plasmids, pcDNA3.1/Hygro expression vector containing immunogenic sequences of fused p24-gp41 or gp41alone were produced. Dendrosome used as a system for carrying vectors in laboratory animals, and an IL-12 containing vector (pCAGGS-IL-12) was co-immunized with the p24-gp41 vector as a genetic adjuvant. Induction of effective immune responses against the designed vectors as DNA vaccine candidates in Balb/c mice was evaluated. Levels of total antibodies, IgG isotypes (IgG2a and IgG1); IFN-γ and IL-4 were measured by ELISA. MTT assay was used to evaluate lymphoproliferation. Results: The results confirmed that the immunogenic epitopes of both p24 and gp41 genes are highly effective inducers of immune responses, and administration of fused p24-gp41 alone or along with IL-12 resulted in further enhancement of immune responses. Group 4 that received fused fragments (p24-gp41) along with an IL-12 expressing vector demonstrated a significantly higher Stimulation Index (SI) and IFN-γ production (p
Databáze: OpenAIRE