Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Dermatology, Harvard Medical School, Boston, Massachusetts, USA.
Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, Massachusetts, USA; Department of Dermatology, Harvard Medical School, Boston, Massachusetts, USA; The first affiliated Hospital, Sun Yat-Sen University, Sun Yat-Sen University, Guangzhou, China.
J Invest Dermatol. 2023 Oct;143(10):1983-1992.e3. doi: 10.1016/j.jid.2023.03.1672. Epub 2023 Apr 11.
Microneedle array has proven more efficient in stimulating humoral immunity than intramuscular vaccination. However, its effectiveness in inducing pulmonary CD8+ T cells remains elusive, which is essential to the frontline defense against pulmonary viral infections such as influenza and COVID-19 viruses. The current investigation reveals that superior CD8+ T-cell responses are elicited by immunization with a microneedle array over intradermal or intramuscular immunization using the model antigen ovalbumin, irrespective of whether or not the antigen is provided in the lung. Mechanistically, microneedle array-mediated immunization targeted the epidermal layer and stimulated predominantly Langerhans cells, resulting in increased expression of α4β1 adhesion molecules on the CD8+ T-cell surface, which may play a role in T-cell homing to the lung, whereas CD8+ T cells induced by intramuscular immunization did not express the adhesion molecule sufficiently. CD8+ T cells with a lung-homing propensity were also seen after intradermal vaccination, yet to a much lesser extent. Accordingly, microneedle array immunization provided stronger protection against influenza viral infection than intradermal or intramuscular immunization. The observations offer insights into a strong cross-talk between epidermal immunization and lung immunity and are valuable for designing and delivering vaccines against respiratory viral infections.
微针阵列已被证明在刺激体液免疫方面比肌肉内接种更有效。然而,其在诱导肺部 CD8+T 细胞方面的效果仍不清楚,而诱导肺部 CD8+T 细胞对于预防流感和 COVID-19 等肺部病毒感染至关重要。本研究表明,与使用模型抗原卵清蛋白进行皮内或肌肉内免疫相比,使用微针阵列进行免疫可引发更强的 CD8+T 细胞反应,无论抗原是否在肺部提供。从机制上讲,微针阵列介导的免疫针对表皮层并主要刺激朗格汉斯细胞,导致 CD8+T 细胞表面 α4β1 粘附分子的表达增加,这可能在 T 细胞归巢到肺部中起作用,而肌肉内免疫诱导的 CD8+T 细胞则不能充分表达粘附分子。皮内接种后也观察到具有肺部归巢倾向的 CD8+T 细胞,但程度要低得多。因此,微针阵列免疫接种比皮内或肌肉内免疫接种能提供更强的流感病毒感染保护。这些观察结果提供了对表皮免疫与肺部免疫之间强烈相互作用的深入了解,对于设计和递送针对呼吸道病毒感染的疫苗具有重要价值。