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Showing 3 results for Haji Molla Hoseini

Maryam Moradi, Mostafa Haji Molla Hoseini, Somayeh Ghotloo, Vahid Khaze,
Volume 38, Issue 1 (4-2014)
Abstract

Abstract Background: There are contradictions about the immune modulating properties of chitin in comparison with chitosan. To respond to these contradictions, we investigated stimulatory effects of chitin micro-particles in comparison with chitosan micro-particles on L.major infected cell suspensions. Materials and methods: In this experimental study, Balb/c mice were intradermally infected with 2 × 105 stationary phase of L.major promastigotes into their base of the tail.Two weeks later infectivity were confirmed by PCR then leishmania infected lymph nodes cell suspensions of the mice were isolated. Chitin micro-particles were prepared by sonication and passing the filter and after size determination by mastersizer, used for cell stimulation.Finally,ELISA measured concentrations of TNF-α and IL-10 in cell culture supernatants. Results: We observed chitin micro-particles significantly increase TNF-αand also IL-10 production (P ≤0.001) in compare with chitosan. Conclusion: Chitin micro-particles can stimulate production of TNF-α and IL-10 in leishmania infected cell suspensions. Chitin seems to be utilized as an immunomodulator in Leishmania vaccine or treatment. 


Mostafa Haji Molla Hoseini,, Somayeh Ghotloo, Vahid Khaze,
Volume 39, Issue 1 (5-2015)
Abstract

Background: Chitin micro-particles have the ability to modulate immune responses. In order to investigate the  immunoadjuvant potential of chitin, the parasite burden in Balb/c mice infected with Leishmania Major under treatment with chitin microparticles was evaluated. In measuring the parasitic load, titration method, which is the most accurate assessment of the effectiveness of therapies and vaccine evaluation in experimental models of Leishmania infection was used.

 Methods: Balb/c mice were intradermally infected with 2 × 105 stationary phase of Leishmania Major promastigotes into their base of the tail and eight weeks later, parasite burden were measured and compared between test (6 mice/group) that recived 100 μg/ml microparticle subcutaneously at the base of the tail every two days and control groups (6 mice/group) that received PBS. The onset and size of ulcer  among two groups were compared as well.

Results: Onset of ulcers in the treated mice compared to control showed a significant delay (p<0.02) and the lesion development in the micro-particle recipient mice were significantly smaller. Although the parasite load in treated mice was lower but statistically significant differences were not found between the test group and control (p<0.88).

Conclusion: The combined use of monitoring the size of the cutaneous lesions and the determination of the parasite burden will reflect more accurately the status of disease. Although the removal of the viseralized parasite was not found among  chitin trated group, but onset and size of ulcer was impressed.  Immunoadjuvant effects of chitin microparticles in Leishmania infection  models requires further studies.


Mahdieh Azizi, Roya Yousefi, Farshid Yeganeh, Mostafa Haji Molla Hoseini,
Volume 43, Issue 2 (7-2019)
Abstract

Background: There are reports on the ability of chitin microparticles to modulate the TH1 and TH2
responses, depending on the size and administration route. The purpose of the present study was to
investigate the immunoadjuvant effects of the small-sized (less than 40 microns) chitin microparticles
(CMP) in vaccination against Leishmania major for preventing leishmaniasis in BALB /c mice by
determining IgG1 and IgG2a.
Methods: BALB⁄c mice in test and control groups (6 mice per group), during 21 days were immunized
subcutaneously three times with soluble Leishmania antigens (SLA) or SLA/CMP. Three weeks after the
last immunization, blood sampling was performed and immunoglobulin isotype was determined using
ELISA. Then 2 × 105 L. major promastigotes were injected into the base of the tail of the mice. Next, onset
and size of the lesions were measured in each group. In the eighth week, blood samples were obtained from
the eye for evaluation of IgG1 and IgG2a level and then the mice were sacrificed and their lymph nodes
were isolated to determine the parasitic burden using Limiting dilution assay (LDA).
Results: The SLA / CMP-immunized mice in compared to the non-immunization group, the onset of the
wound were postponed and the parasitic load [(0.41±3.9 Vs.0.82±5.8 Log (Parasites per lymph node)]
(P≤0.05) and the extended area of the wound (P≤0.007) were significantly decreased. The results of
the serum IgG1 and IgG2a assay showed that immunization by chitin microparticles caused significant
decrease in the serum IgG1 level before (P≤0.001) and after (P≤0.014) the challenge but not IgG2a.
Conclusion: Co-administration of CMP/SLA cause significant inhibition of IgG1 responses. It seems that
CMP could downregulate unbridled TH2 response in Leishmania infection.



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