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Written and prepared by:
Styliani Karanika, James T. Gordy, Pranita Neupane, Theodoros Karantanos, Jennie Ruelas Castillo, Darla Quijada, Kaitlyn Comstock, Avinaash Kaur Sandhu, Yinan Hui, Samuel K. Ayeh, Rokeya Tasneen, Stefanie Krug, Carina Danchik, Tianyin Wang, Courtney Schill, Rirchard B. Markham, Petros C. Karakousis
Discover an intranasal stringent response vaccine targeting dendritic cells for tuberculosis therapy. This novel approach enhances the efficacy of standard treatment by inducing robust Th1 and Th17 immune responses. The fusion of the relMtb gene with the chemokine MIP-3α/CCL20 and intranasal delivery significantly improves mycobactericidal activity, reducing lung bacterial burden in a murine model of chronic TB. The study suggests this vaccination strategy as a promising adjunctive therapy for TB.
Novel intranasal DNA vaccine targeting dendritic cells for tuberculosis therapy.
Study explores how DNA vaccines can enhance the efficacy of tuberculosis treatments.
Analysis of immune responses triggered by MIP-3α/relMtb fusion vaccine for TB.
Investigating the combined use of MIP-3α fusion and intranasal routes for TB vaccines.
Study shows intranasal vaccination induces strong Th1 and Th17 responses against TB.
Combining MIP-3α fusion and intranasal delivery enhances TB vaccine efficacy.
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