A New Approach for Development of Vaccine Against Visceral Leishmaniasis: Lipophosphoglycan and Polyacrylic Acid Conjugates

Loading...
Publication Logo

Date

2017

Journal Title

Journal ISSN

Volume Title

Publisher

Wolters Kluwer Medknow Publications

Open Access Color

GOLD

Green Open Access

Yes

OpenAIRE Downloads

3

OpenAIRE Views

3

Publicly Funded

No
Impulse
Average
Influence
Average
Popularity
Top 10%

Research Projects

Journal Issue

Abstract

Objective: To determine the antileishmanial vaccine effectiveness of lipophosphoglycan (LPG) and polyacrylic acids (PAA) conjugates on in vivo mice models. Methods: LPG molecule was isolated and purified from large-scale Leishmania donovani parasite culture. Protection efficacies of LPG alone, in combination with Freund's adjuvant, in a physical mixture and in conjugate (consisting of various LPG concentrations) with PAA, were comparatively determined by various techniques, such as cultivation with the micro-culture method, assessment of in vitro infection rates of peritoneal macrophages, determination of parasite load in liver with Leishman-Donovan Units, and detection of cytokine responses. Results: Obtained results demonstrated that the highest vaccine-mediated immune protection was provided by LPG-PAA conjugate due to all parameters investigated. According to the Leishman-Donovan Units results, the sharpest decline in parasite load was seen with a ratio of 81.17% when 35 mg LPG containing conjugate was applied. This value was 44.93% for the control group immunized only with LPG. Moreover, decreases in parasite load were 53.37%, 55.2% and 65.8% for the groups immunized with 10 mg LPG containing LPG-PAA conjugate, a physical mixture of the LPG-PAA, and a mixture of LPG + Freund's adjuvant, respectively. Furthermore, cytokine results supported that Th1 mediated protection occurred when mice were immunized with LPG-PAA conjugate. Conclusions: It has been demonstrated in this study that conjugate of LPG and PAA has an antileishmanial vaccine effect against visceral leishmaniasis. In this respect, the present study may lead to new vaccine approaches based on high immunogenic LPG molecule and adjuvant polymers in fighting against Leishmania infection.

Description

Dincer Isoglu, Sevil/0000-0002-6887-6549; Cakir, Rabia/0000-0002-8545-9878; Allahverdiyev, Adil M./0000-0002-7031-5986; Yesilkir Baydar, Serap/0000-0001-6311-4302; Mustafaeva, Zeynep/0000-0002-4352-7617; Canim Ates, Sezen/0000-0003-2196-7053; Topuzogullari, Murat/0000-0003-4435-7776

Keywords

Leishmania, LipoPhosphoglycan, Vaccine, Polymer, Polyacrylic Acid, Leishmania, Lipophosphoglycan, Polymer, Vaccine, Polyacrylic acid

Fields of Science

03 medical and health sciences, 0302 clinical medicine

Citation

WoS Q

Q3

Scopus Q

Q2
OpenCitations Logo
OpenCitations Citation Count
12

Source

Asian Pacific Journal of Tropical Medicine

Volume

10

Issue

9

Start Page

877

End Page

886
PlumX Metrics
Citations

CrossRef : 11

Scopus : 15

PubMed : 4

Captures

Mendeley Readers : 53

SCOPUS™ Citations

15

checked on Apr 14, 2026

Web of Science™ Citations

14

checked on Apr 14, 2026

Page Views

5

checked on Apr 14, 2026

Downloads

4

checked on Apr 14, 2026

Google Scholar Logo
Google Scholar™
OpenAlex Logo
OpenAlex FWCI
1.1781

Sustainable Development Goals

SDG data is not available