IP Library › Granted Patent US 11,834,647
Granted Patent B2
US 11,834,647 · App. 17/021,158 · Granted Dec 5, 2023

In vitro immune synapse system and method of in vitro evaluating immune response using the same

Inventors: Hso-Chi Chaung (Neipu, TW); Wen-Bin Chung (Neipu, TW); Ann Ying-An Chen (Neipu, TW); Mei-Li Wu (Neipu, TW)
Assignee: National Pingtung University of Science and Technology
C12N5/0638A01K67/0278C12N5/0637C12N5/0645C12N5/0646G01N33/5047G01N33/6869A01K2207/15A01K2217/206A01K2227/108A01K2267/0387
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Quick Facts
Patent No.
US 11,834,647
App. No.
17/021,158
Granted
Dec 5, 2023
Kind
B2
Abstract

The present invention relates to an in vitro immune synapse system and a method of in vitro evaluating immune response using the same. The in vitro immune synapse system includes antigen-presenting cells (APCs) and at least one cell type of several specific T cell subtypes isolated from peripheral blood mononuclear cells (PBMCs), all of which is from a same individual of pigs. When a test sample is co-cultured in the in vitro immune synapse system for a given period, it can be determined that the test sample is immunogenic, immunostimulatory or not according to the immunization-related changes of these cells, thereby potentially replacing some kinds of animal experimentation.

Claims (14)

1. A method of in vitro evaluating immune response, comprising:

providing an in vitro immune synapse system, wherein the in vitro immune synapse system comprises:

an antigen-presenting cell, wherein the antigen-presenting cell is an alveolar macrophage;

at least one of a regulatory T cell, a killer cell and a helper T cell, wherein the regulatory T cell has at least a CD4+/CD25+ cell marker, the killer cell has at least a CD4−/CD25+ cell marker, the helper T cell has at least a CD4+/CD25− cell marker; and

a control cell, wherein the control cell has at least a CD4−/CD25− cell marker, and

wherein the antigen-presenting cell, the regulatory T cell, the killer cell, the helper T cell and the control cell are primary cell derived from a same individual, and a number of the antigen-presenting cell is 2 to 10 times of a total number of the regulatory T cell, the killer cell and the helper T cell;

co-culturing a test sample in the immune synapse system for 24 hours; and

detecting the immune synapse system for an immunization-related change, wherein the immunization-related change comprises a level of toll-like receptor (TLR) gene expression, and

wherein when any one of the regulatory T cell, the killer cell, the helper T cell has its immunization-related change significantly differ from the immunization-related change of the control cell, the test sample is determined to be immunogenic or immunostimulatory in a porcine respiratory mucosa immune system.

2. The method of in vitro evaluating immune response of claim 1 , wherein the test sample comprises an antigen or an adjuvant.

3. The method of in vitro evaluating immune response of claim 1 , wherein the same individual is a SPF pig.

4. The method of in vitro evaluating immune response of claim 1 , wherein the TLR gene expression level comprises a TLR3 gene expression level, a TLR7 gene expression level, and/or a TLR8 gene expression level.

5. The method of in vitro evaluating immune response of claim 1 , wherein the immunization-related change further comprises a cytokine concentration.

6. The method of in vitro evaluating immune response of claim 5 , wherein the cytokine concentration comprises an interleukin (IL) concentration.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2020
From: CHAUNG, HSO-CHI; CHUNG, WEN-BIN; CHEN, ANN YING-AN; WU, MEI-LI
To: NATIONAL PINGTUNG UNIVERSITY OF SCIENCE AND TECHNOLOGY
Reel/Frame 053773/0111 →
Continuity (2)
Division 16219006 · Dec 13, 2018
Related Publication 20200407683A1 · Dec 31, 2020