Immunotherapy of Fungal Infections

被引:27
作者
Datta, Kausik [1 ]
Hamad, Mawieh [2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Infect Dis, 720 Rutland Ave,Ross Res Bldg,Ste 1064, Baltimore, MD 21211 USA
[2] Univ Sharjah, Dept Med Lab Sci, Sharjah, U Arab Emirates
[3] Univ Sharjah, Sharjah Inst Med Res, Sharjah, U Arab Emirates
关键词
Antifungal; antigen; fungal infection; fungal vaccine; immunotherapy; invasive mycosis; COLONY-STIMULATING FACTOR; MOBILIZED GRANULOCYTE TRANSFUSIONS; KILLER ANTIIDIOTYPIC ANTIBODY; HUMAN RECOMBINANT ANTIBODY; ENHANCE MOUSE RESISTANCE; BETA-GLUCAN ANTIBODIES; NECROSIS-FACTOR-ALPHA; KEY SIGNALING ENZYME; CRYPTOCOCCUS-NEOFORMANS; CANDIDA-ALBICANS;
D O I
10.3109/08820139.2015.1093913
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fungal organisms are ubiquitous in the environment. Pathogenic fungi, although relatively few in the whole gamut of microbial pathogens, are able to cause disease with varying degrees of severity in individuals with normal or impaired immunity. The disease state is an outcome of the fungal pathogen's interactions with the host immunity, and therefore, it stands to reason that deep/invasive fungal diseases be amenable to immunotherapy. Therefore, antifungal immunotherapy continues to be attractive as an adjunct to the currently available antifungal chemotherapy options for a number of reasons, including the fact that existing antifungal drugs, albeit largely effective, are not without limitations, and that morbidity and mortality associated with invasive mycoses are still unacceptably high. For several decades, intense basic research efforts have been directed at development of fungal immunotherapies. Nevertheless, this approach suffers from a severe bench-bedside disconnect owing to several reasons: the chemical and biological peculiarities of the fungal antigens, the complexities of host-pathogen interactions, an under-appreciation of the fungal disease landscape, the requirement of considerable financial investment to bring these therapies to clinical use, as well as practical problems associated with immunizations. In this general, non-exhaustive review, we summarize the features of ongoing research efforts directed towards devising safe and effective immunotherapeutic options for mycotic diseases, encompassing work on antifungal vaccines, adoptive cell transfers, cytokines, antimicrobial peptides (AMPs), monoclonal antibodies (mAbs), and other agents.
引用
收藏
页码:738 / 776
页数:39
相关论文
共 225 条
[31]   Antibody-mediated protection through cross-reactivity introduces a fungal heresy into immunological dogma [J].
Casadevall, Arturo ;
Pirofski, Lilse-anne .
INFECTION AND IMMUNITY, 2007, 75 (11) :5074-5078
[32]   Immunoglobulins in Defense, Pathogenesis, and Therapy of Fungal Diseases [J].
Casadevall, Arturo ;
Pirofski, Liise-anne .
CELL HOST & MICROBE, 2012, 11 (05) :447-456
[33]   Modulation of phenotype and function of dendritic cells by a therapeutic synthetic killer peptide [J].
Cenci, E ;
Pericolini, E ;
Mencacci, A ;
Conti, S ;
Magliani, W ;
Bistoni, F ;
Polonelli, L ;
Vecchiarelli, A .
JOURNAL OF LEUKOCYTE BIOLOGY, 2006, 79 (01) :40-45
[34]   A synthetic peptide as a novel anticryptococcal agent [J].
Cenci, E ;
Bistoni, F ;
Mencacci, A ;
Perito, S ;
Magliani, W ;
Conti, S ;
Polonelli, L ;
Vecchiarelli, A .
CELLULAR MICROBIOLOGY, 2004, 6 (10) :953-961
[35]   Protection of killer antiidiotypic antibodies against early invasive aspergillosis in a murine model of allogeneic T-cell-depleted bone marrow transplantation [J].
Cenci, E ;
Mencacci, A ;
Spreca, A ;
Montagnoli, C ;
Bacci, A ;
Perruccio, K ;
Velardi, A ;
Magliani, W ;
Conti, S ;
Polonelli, L ;
Romani, L .
INFECTION AND IMMUNITY, 2002, 70 (05) :2375-2382
[36]   T cell vaccination in mice with invasive pulmonary aspergillosis [J].
Cenci, E ;
Mencacci, A ;
Bacci, A ;
Bistoni, F ;
Kurup, VP ;
Romani, L .
JOURNAL OF IMMUNOLOGY, 2000, 165 (01) :381-388
[37]   Voriconazole inhibition of tacrolimus metabolism in a kidney transplant recipient with fluconazole-resistant cryptococcal meningitis [J].
Chang, Hui-Hua ;
Lee, Nan-Yao ;
Ko, Wen-Chien ;
Lee, Hsin-Chun ;
Yang, Yea-Hui Kao ;
Wu, Chi-Jung ;
Chang, Chia-Ming .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2010, 14 (04) :E348-E350
[38]   Blockade ofthe negative co-stimulatory molecules PD-1 and CTLA-4 improves survival in primary and secondary fungal sepsis [J].
Chang, Katherine C. ;
Burnham, Carey-Ann ;
Compton, Stephanie M. ;
Rasche, David P. ;
Mazuski, Richard J. ;
McDonough, Jacquelyn S. ;
Unsinger, Jacqueline ;
Korman, Alan J. ;
Green, Jonathan M. ;
Hotchkiss, Richard S. .
CRITICAL CARE, 2013, 17 (03)
[39]   Monoclonal immunoglobulin G1 directed against Aspergillus fumigatus cell wall glycoprotein protects against experimental murine aspergillosis [J].
Chaturvedi, AK ;
Kavishwar, A ;
Keshava, GBS ;
Shukla, PK .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2005, 12 (09) :1063-1068
[40]   Vaccine-Mediated Immune Responses to Experimental Pulmonary Cryptococcus gattii Infection in Mice [J].
Chaturvedi, Ashok K. ;
Hameed, Rumanasma S. ;
Wozniak, Karen L. ;
Hole, Camaron R. ;
Wager, Chrissy M. Leopold ;
Weintraub, Susan T. ;
Lopez-Ribot, Jose L. ;
Wormley, Floyd L., Jr. .
PLOS ONE, 2014, 9 (08)