Co-administration of immunomodulator tuftsin and liposomised nystatin can combat less susceptible Candida albicans infection in temporarily neutropenic mice

In order to develop a prospective chemotherapeutic agent against opportunistic infections, it is important to know that host factors such as degree of immunological debility as well as recovery of immune functions to normality may contribute significantly to a successful elimination of the pathogens...

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Published inFEMS immunology and medical microbiology Vol. 41; no. 3; pp. 249 - 258
Main Authors Khan, Masood A, Nasti, T.H, Saima, Khanam, Mallick, A.I, Firoz, Ahmad, Wajahul, Haq, Ahmad, Nadeem, Mohammad, Owais
Format Journal Article
LanguageEnglish
Published Oxford, UK Elsevier B.V 01.07.2004
Blackwell Publishing Ltd
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Oxford University Press
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Abstract In order to develop a prospective chemotherapeutic agent against opportunistic infections, it is important to know that host factors such as degree of immunological debility as well as recovery of immune functions to normality may contribute significantly to a successful elimination of the pathogens. We demonstrated previously that concomitant delivery of antimicrobial agents and immunomodulators to the pathogen harbouring-host contributes to the complete elimination of the deep-seated fungal infections (aspergillosis and candidiasis) in animals with normal immune status. Considering that neutropenic hosts are the main targets of such infections, it can be argued about the potential of the immunomodulator-based therapy in subjects with non-functional immune system. To resolve the hypothesis, we studied the role of immunomodulator tuftsin against experimental murine candidiasis in temporarily neutropenic Balb/c mice. The neutropenic mice were challenged with an isolate of Candida albicans that was showing less susceptibility to both free and liposomised-amphotericin B. The co-administration of tuftsin increased the efficiency of liposomised-polyene antibiotics (nystatin and amphotericin B) against experimental murine candidiasis in immunocompromised Balb/c mice. Pretreatment with liposomised tuftsin prior to C. albicans infection clearly enhanced protection against candidiasis, suggesting a prophylactic role of tuftsin in normal and temporarily neutropenic animals.
AbstractList In order to develop a prospective chemotherapeutic agent against opportunistic infections, it is important to know that host factors such as degree of immunological debility as well as recovery of immune functions to normality may contribute significantly to a successful elimination of the pathogens. We demonstrated previously that concomitant delivery of antimicrobial agents and immunomodulators to the pathogen harbouring‐host contributes to the complete elimination of the deep‐seated fungal infections (aspergillosis and candidiasis) in animals with normal immune status. Considering that neutropenic hosts are the main targets of such infections, it can be argued about the potential of the immunomodulator‐based therapy in subjects with non‐functional immune system. To resolve the hypothesis, we studied the role of immunomodulator tuftsin against experimental murine candidiasis in temporarily neutropenic Balb/c mice. The neutropenic mice were challenged with an isolate of Candida albicans that was showing less susceptibility to both free and liposomised‐amphotericin B. The co‐administration of tuftsin increased the efficiency of liposomised‐polyene antibiotics (nystatin and amphotericin B) against experimental murine candidiasis in immunocompromised Balb/c mice. Pretreatment with liposomised tuftsin prior to C. albicans infection clearly enhanced protection against candidiasis, suggesting a prophylactic role of tuftsin in normal and temporarily neutropenic animals.
In order to develop a prospective chemotherapeutic agent against opportunistic infections, it is important to know that host factors such as degree of immunological debility as well as recovery of immune functions to normality may contribute significantly to a successful elimination of the pathogens. We demonstrated previously that concomitant delivery of antimicrobial agents and immunomodulators to the pathogen harbouring-host contributes to the complete elimination of the deep-seated fungal infections (aspergillosis and candidiasis) in animals with normal immune status. Considering that neutropenic hosts are the main targets of such infections, it can be argued about the potential of the immunomodulator-based therapy in subjects with non-functional immune system. To resolve the hypothesis, we studied the role of immunomodulator tuftsin against experimental murine candidiasis in temporarily neutropenic Balb/c mice. The neutropenic mice were challenged with an isolate of Candida albicans that was showing less susceptibility to both free and liposomised-amphotericin B. The co-administration of tuftsin increased the efficiency of liposomised-polyene antibiotics (nystatin and amphotericin B) against experimental murine candidiasis in immunocompromised Balb/c mice. Pretreatment with liposomised tuftsin prior to C. albicans infection clearly enhanced protection against candidiasis, suggesting a prophylactic role of tuftsin in normal and temporarily neutropenic animals.
Abstract In order to develop a prospective chemotherapeutic agent against opportunistic infections, it is important to know that host factors such as degree of immunological debility as well as recovery of immune functions to normality may contribute significantly to a successful elimination of the pathogens. We demonstrated previously that concomitant delivery of antimicrobial agents and immunomodulators to the pathogen harbouring-host contributes to the complete elimination of the deep-seated fungal infections (aspergillosis and candidiasis) in animals with normal immune status. Considering that neutropenic hosts are the main targets of such infections, it can be argued about the potential of the immunomodulator-based therapy in subjects with non-functional immune system. To resolve the hypothesis, we studied the role of immunomodulator tuftsin against experimental murine candidiasis in temporarily neutropenic Balb/c mice. The neutropenic mice were challenged with an isolate of Candida albicans that was showing less susceptibility to both free and liposomised-amphotericin B. The co-administration of tuftsin increased the efficiency of liposomised-polyene antibiotics (nystatin and amphotericin B) against experimental murine candidiasis in immunocompromised Balb/c mice. Pretreatment with liposomised tuftsin prior to C. albicans infection clearly enhanced protection against candidiasis, suggesting a prophylactic role of tuftsin in normal and temporarily neutropenic animals.
Author Saima, Khanam
Ahmad, Nadeem
Nasti, T.H
Firoz, Ahmad
Mohammad, Owais
Mallick, A.I
Khan, Masood A
Wajahul, Haq
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Issue 3
Keywords Immunomodulator
Liposome
Candidiasis
Nystatin
Tuftsin
Candida albicans
Yeast
Leukopenia
Mycosis
Microbiology
Rodentia
Hemopathy
Fungi
Infection
Vertebrata
Antifungal agent
Mammalia
Immunology
Mouse
Fungi Imperfecti
Thallophyta
Neutropenia
Language English
License CC BY 4.0
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Notes Interdisciplinary Biotechnology Unit, AMU, Aligarh, India.
Jamia Hamdard, New Delhi‐62, India.
Central Drug Research Institute, Lko, India.
ICGEB, Shaheed Jeet Singh Marg, New Delhi, India.
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Snippet In order to develop a prospective chemotherapeutic agent against opportunistic infections, it is important to know that host factors such as degree of...
Abstract In order to develop a prospective chemotherapeutic agent against opportunistic infections, it is important to know that host factors such as degree of...
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SubjectTerms Adjuvants, Immunologic - administration & dosage
Amphotericin B
Animals
Antibiotics
Antifungal agents
Antifungal Agents - administration & dosage
Antimicrobial agents
Aspergillosis
Biological and medical sciences
Candida albicans
Candida albicans - pathogenicity
Candidiasis
Candidiasis - drug therapy
Candidiasis - immunology
Candidiasis - microbiology
Candidiasis - prevention & control
Drug Synergism
Drug Therapy, Combination
Female
Fundamental and applied biological sciences. Psychology
Immune status
Immune system
Immunology
Immunomodulation
Immunomodulator
Immunomodulators
Infections
Liposome
Liposomes - administration & dosage
Mice
Mice, Inbred BALB C
Microbiology
Miscellaneous
Mycology
Neutropenia
Neutropenia - complications
Normality
Nystatin
Nystatin - administration & dosage
Pathogens
Pretreatment
Treatment Outcome
Tuftsin
Tuftsin - administration & dosage
Title Co-administration of immunomodulator tuftsin and liposomised nystatin can combat less susceptible Candida albicans infection in temporarily neutropenic mice
URI https://dx.doi.org/10.1016/j.femsim.2004.03.011
https://onlinelibrary.wiley.com/doi/abs/10.1016%2Fj.femsim.2004.03.011
https://www.ncbi.nlm.nih.gov/pubmed/15196575
https://www.proquest.com/docview/2307185103
https://search.proquest.com/docview/18031841
Volume 41
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