CD28 (Cluster of Differentiation 28) is a homodimeric stimulatory cell surface receptor of the immunoglobulin (Ig) superfamily that is located on the chromosome 2q33.2. It is expressed on naive T cells and has also been found on the surface of plasma cells, eosinophils, and neutrophils. CD28 remains the most extensively studied costimulatory molecular and is a primary one for T-cell activatio. The control of T-cell responses through CD28 co-stimulation provides a means of anti-self and antimicrobial immunity. CD28 is essential for the lymphocyte activation and survival. A number of antigen-experienced T-cells lose CD28, and then can be re-activated without its engagement. Diseases linked to CD28 involve mycosis fungoides and Sezary's disease and the related pathways are Th2 differentiation pathway and RET signaling. CD3 (Cluster of differentiation 3), originally known as T3, is one of the first groups of human T lymphocyte surface antigens recognized by monoclonal antibodies. It has been reported that antibodies against CD3 could either stimulate T cells to divide or inhibit the progress of effector functions according to the conditions used. It plays an important role in T cell and the CD3 T-cell co-receptor helps to activate the cytotoxic T-Cell and T helper cells. The CD3 molecule is composed of a protein complex and consists of four distinct chains. The complex of mammals contains a CD3γ chain, a CD3δ chain, and two CD3ε chains. All these chains associate with T-cell receptor and the ζ-chain to generate an activation signal in T lymphocytes.