Development Center for Biotechnology

Academia Sinica

National Health Research Institutes

Dcb-usa LLC

Chih-Yung Hu

Szu-Liang Lai

Ying-Yung Lok

Chun-Chung Lee

Ko-Jiunn Liu

Yuan-Tsong Chen

Neng-Yao Shih

Chu-Bin Liao

Ta-Tung Yuan

Chao-Yang Huang

Jiann-Shiun Lai

Shih-Chong Tsai

Li-Tzong Chen

Chia-Cheng Wu

Shih-Chi Tseng

Woan-Eng Chan

Chung-Hsiun Wu

Hong-Kai Chen

Chien-Tsun Kuan

Yen-Yu Wu

Hsin-Yun Wang

Wen-Bin Ke

Yu-Hsun Lo

Chen-Jei Hong

Kao-Jean Huang

Sih-Yu Chen

Ya-Ting Juan

Hung-Ling Wang

Pei-Han Tai

Chia-Hua Li

Li-Yu Chen

Yu-Chen Yang

Tzu-Yin Lin

Yu-Jung Chen

The present invention relates to a novel antibody, an antigen-binding fragment thereof and the uses of the antibody and fragment, wherein the antibody and the fragment comprise specific complementarity-determining regions (CDRs) and/or specifically bind to human CD73 at specific epitopes.

Anti-CD73 antibodies and use thereof

A humanized anti-Globo H antibody, or an scFv or Fab fragment thereof, comprising a heavy-chain variable domain having three complementary regions consisting of HCDR1, HCDR2, and HCDR3 and a light-chain variable domain having three complementary regions consisting of LCDR1, LCDR2, and LCDR3, wherein the sequence of HCDR1 is GYISSDQILN (SEQ ID NO:4), the sequence of HCDR2 is RIYPVTGVTQYXHKFVG (SEQ ID NO:5, wherein X is any amino acid), and the sequence of HCDR3 is GETFDS (SEQ ID NO:6), wherein the sequence of LCDR1 is KSNQNLLX'SGNRRYZLV (SEQ ID NO:7, wherein X&#x2032; is F, Y, or W, and Z is C, G, S or T), the sequence of LCDR2 is WASDRSF (SEQ ID NO:8), and the sequence of LCDR3 is QQHLDIPYT (SEQ ID NO:9).

Humanized antibodies against Globo H and uses thereof in cancer treatments

An anti-human T-cell immunoglobulin domain and mucin domain 3 (TIM-3) antibody, can bind the peptides, comprising the amino-acid sequence RKGDVSL (SEQ ID NO: 9) and/or EKFNLKL (SEQ ID NO: 10) of human TIM-3 protein. The antibody can regulate immune cell activity. The antibody or binding fragment thereof is useful in diagnosis, prognosis, and treatment of cancers that have been reported to express cell-surface TIM-3 such as lung, liver, esophageal cancer and solid tumors.

Anti-human TIM-3 antibodies and methods of use thereof

An anti-granulysin antibody, or an scFv or Fab fragment thereof, capable of binding to an epitope region from R64 to R113 of granulysin and capable of neutralizing an activity of granulysin. The antibody may contain a sequence selected from the sequences of SEQ ID NO:82 to SEQ ID NO:195, or the antibody may contain a sequence selected from the sequences of SEQ ID NO:39 to SEQ ID NO:76. The antibody may be a monoclonal antibody. A method for treating or preventing an unwanted immune response disorder includes administering to a subject in need thereof an effective amount of an anti-granulysin antibody capable of neutralizing the activity of granulysin. The unwanted immune response disorder may be SJS, TEN, or GVHD.

Anti-granulysin antibodies and methods of use thereof

The present invention discloses an anti-human alpha-enolase (ENO1) antibody, which can bind the peptides, comprising amino-acid sequence 296FD Q D D W G A W Q K F TA309 (SEQ ID: #9) and/or 326K R I A K A V N EK S336 (SEQ ID: #10) of human ENO1 protein (GenBank: AAH50642.1), has a favorable binding activity (the binding affinity is around 2.19&#xd7;10-10 mol/L) and a remarkable capability to inhibit the cell invasion and tumor metastasis of a varied of tumors. The recognized peptides and antibody of the invention are useful for diagnosis, prognosis, and treatment of cancers that have been reported to express cell-surface ENO1 such as including lung, breast, pancreas, liver, colorectal, prostate cancers and solid tumors.

Alpha-enolase specific antibodies and methods of uses in cancer therapy

Growing community of inventors

Taipei, Taiwan

Chih-Yung Hu