Mucosal vaccines: a paradigm shift in the development of mucosal adjuvants and delivery vehicles

被引:49
作者
Srivastava, Atul [1 ]
Gowda, Devegowda Vishakante [1 ]
Madhunapantula, SubbaRao V. [2 ]
Shinde, Chetan G. [1 ]
Iyer, Meenakshi [3 ]
机构
[1] JSS Univ, Dept Pharmaceut, JSS Coll Pharm, Mysore 570015, Karnataka, India
[2] JSS Univ, Dept Biochem, JSS Med Coll, Mysore 570015, Karnataka, India
[3] JSS Univ, Dept Prosthodont, JSS Dent Coll & Hosp, Mysore 570015, Karnataka, India
关键词
Mucosal vaccines; mucosal adjuvant; antigen delivery; immune response; MONOPHOSPHORYL-LIPID-A; RECONSTITUTED INFLUENZA VIROSOMES; ANTIGEN-PRESENTING CELLS; INTRANASAL IMMUNIZATION; IMMUNE-RESPONSES; DRUG-DELIVERY; CHOLERA-TOXIN; ORAL VACCINE; PROTECTIVE IMMUNITY; NASAL IMMUNIZATION;
D O I
10.1111/apm.12351
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mucosal immune responses are the first-line defensive mechanisms against a variety of infections. Therefore, immunizations of mucosal surfaces from which majority of infectious agents make their entry, helps to protect the body against infections. Hence, vaccinization of mucosal surfaces by using mucosal vaccines provides the basis for generating protective immunity both in the mucosal and systemic immune compartments. Mucosal vaccines offer several advantages over parenteral immunization. For example, (i) ease of administration; (ii) non-invasiveness; (iii) high-patient compliance; and (iv) suitability for mass vaccination. Despite these benefits, to date, only very few mucosal vaccines have been developed using whole microorganisms and approved for use in humans. This is due to various challenges associated with the development of an effective mucosal vaccine that can work against a variety of infections, and various problems concerned with the safe delivery of developed vaccine. For instance, protein antigen alone is not just sufficient enough for the optimal delivery of antigen(s) mucosally. Hence, efforts have been made to develop better prophylactic and therapeutic vaccines for improved mucosal Th1 and Th2 immune responses using an efficient and safe immunostimulatory molecule and novel delivery carriers. Therefore, in this review, we have made an attempt to cover the recent advancements in the development of adjuvants and delivery carriers for safe and effective mucosal vaccine production.
引用
收藏
页码:275 / 288
页数:14
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