A scFv Phage Display Mini Library Generated from the Immunoglobulin Repertoire of Breast Medullary Carcinoma Infiltrating B Lymphocytes

نویسندگان

  • B. Kotlan
  • P. Simsa
  • N. Gruel
  • J. Foldi
  • W. H. Fridman
  • G. Petranyi
  • J. L. Teillaud
چکیده

The detection and characterization of antigens expressed during the progression of carcinogenesis is still a major goal for tumour immunology. We describe a possible new way for defining human tumour specific antigens with the use of scFv phage display technology [1]. An attractive hypothesis is that tumour infiltrating lymphocytes (TIL) are accumulated in the tumour tissue because of their unique capacity for recognizing tumour cells [2]. This has been proved in the case of tumour infiltrating T lymphocytes (TIL-T) [3, 4]. In contrast, knowledge about tumour infiltrating B lymphocytes (TIL-B) is very limited [5–7]. In this work we show data on the immunoglobulin repertoire expressed by TIL-B cells from medullary breast carcinoma (MBC). A detailed DNA sequence analysis of immunoglobulin heavy (VH) and light chain

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Construction of Human Recombinant ScFv Phage Libraries from the Advanced Stages of Breast Carcinoma Patients

Advances in the field of antibody engineering, and the emergence of powerful screening technology such as filamentous phage display allowed to generate fully human antibodies with high affinities against virtually any desired target from immune or even naIve human repertoires. As a result, the immunogenicity problems related to applications of nonhuman based recombinant antibodies as therapeuti...

متن کامل

Challenging tumour immunological techniques that help to track cancer stem cells in malignant melanomas and other solid tumours

Aim of the study The arsenal of questions and answers about the minor cancer initiating cancer stem cell (CSC) population put responsible for cancer invasiveness and metastases, has left with an unsolved puzzle. Specific aims of a complex project were partly focused on revealing new biomarkers of cancer. We designed and set up novel techniques to facilitate the detection of cancerous cells. M...

متن کامل

Antigen-driven clonal proliferation, somatic hypermutation, and selection of B lymphocytes infiltrating human ductal breast carcinomas.

Infiltration of B lymphocytes into the tumor tissue of breast cancer patients is a common occurrence, but the role of these cells in the immune response to the tumor is unknown. Heavy B-cell infiltration in medullary breast carcinoma is well documented and associated with a more favorable prognosis, implying a positive role for the humoral immune response in elimination of tumor cells. Variable...

متن کامل

Development of a Hyperimmune Anti-MUC-I Single Chain Antibody Fragments Phage Display Library for Targeting Breast Cancer I

Radioimmunotherapy (RIT) has demonstrated potential for improving clinical cancer therapy. Optimizing the approach has proven difficult thus far. Antibody phage display libraries provide unique molecules that could improve RIT. A phage display library of single chain antibody fragments (scFv) against the MUC-1 mucin molecule, which is expressed on 90% of human breast cancers, was produced from ...

متن کامل

Development of a Hyperimmune Anti-MUC-I Single Chain Antibody Fragments Phage Display Library for Targeting Breast Cancer I

Radioimmunotherapy (RIT) has demonstrated potential for improving clinical cancer therapy. Optimizing the approach has proven difficult thus far. Antibody phage display libraries provide unique molecules that could improve RIT. A phage display library of single chain antibody fragments (scFv) against the MUC-1 mucin molecule, which is expressed on 90% of human breast cancers, was produced from ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره 16  شماره 

صفحات  -

تاریخ انتشار 2000