Francis James N, Durham Stephen R
Upper Respiratory Medicine, National Heart and Lung Institute, Imperial College, London SW3 6LY, UK.
Curr Opin Allergy Clin Immunol. 2004 Dec;4(6):543-8. doi: 10.1097/00130832-200412000-00012.
Inclusion of adjuvants in immunotherapy vaccines are important to enhance immune responses to allergens. This article will cover the recent advances in adjuvant formulations described in published articles primarily over the past 2 years.
Traditionally, allergen immunotherapy preparations utilize aluminium hydroxide as an adjuvant. These have generally proved efficacious and have a good safety profile. However, recent advances in the understanding of immunological mechanisms underlying immunotherapy and in the design of new adjuvants may allow a more rational approach to adjuvant use. One approach is to use adjuvants such as immunostimulatory sequences or monophosphoryl lipid A, which can deviate allergy-associated Th2 immune responses towards a Th1 phenotype. Both of these adjuvants have been used in pilot controlled clinical trials which have demonstrated clinical efficacy and the induction of protective IgG antibodies. Other approaches to improve immunotherapy vaccines include microencapsulation of allergen to allow delivery of the allergen directly to the gut in order to induce immunological tolerance and vaccination with heat-killed mycobacteria.
There is great interest in newly designed adjuvants to improve the efficacy and safety of allergen immunotherapy. A better understanding of immunological mechanisms and further clinical trials utilizing new adjuvants are needed.
在免疫治疗疫苗中加入佐剂对于增强对变应原的免疫反应很重要。本文将主要涵盖过去两年发表文章中描述的佐剂配方的最新进展。
传统上,变应原免疫治疗制剂使用氢氧化铝作为佐剂。这些佐剂一般已证明有效且安全性良好。然而,对免疫治疗潜在免疫机制的理解以及新佐剂设计方面的最新进展可能会使佐剂的使用方法更加合理。一种方法是使用免疫刺激序列或单磷酰脂质A等佐剂,它们可使与过敏相关的Th2免疫反应偏向Th1表型。这两种佐剂都已用于试点对照临床试验,试验证明了其临床疗效以及诱导保护性IgG抗体的能力。改进免疫治疗疫苗的其他方法包括变应原的微囊化,以便将变应原直接递送至肠道以诱导免疫耐受,以及用热灭活分枝杆菌进行疫苗接种。
人们对新设计的佐剂以提高变应原免疫治疗的疗效和安全性非常感兴趣。需要更好地理解免疫机制,并利用新佐剂进行进一步的临床试验。