Question

Nonspecific lymphocytes that spontaneously attack and kill cancer cells and cells

Answer 1

Answer:

Antibodies.

Explanation:

An antibody is a protein produced by the white blood cells of an organism to resist harmful foreign substances, so-called antigens. Once the body has done this once against an antigen, it will usually develop immunity to the disease that the antigen represents. A common vaccination method is to supply the body with small amounts of unknown antigens, thus stimulating the body to produce anti-inflammatory antibodies.  In some cases, antibodies can react to harmless substances, causing an allergic reaction.

Answer 2

Answer:

lymphocytes

Explanation:

These cells provide efficient, specific and long-lasting immunity against microbes and are responsible for acquired immunity. Lymphocytes differentiate into three separate lines: thymic-dependent cells or T lymphocytes that operate in cellular and humoral immunity, B lymphocytes that differentiate into plasma cells to secrete antibodies, and natural killer (NK) cells. T and B lymphocytes are the only lymphoid cells that produce and express specific receptors for antigens.

T Lymphocytes: These cells are involved in the regulation of the immune response and in cell mediated immunity and help B cells to produce antibody (humoral immunity). Mature T cells express antigen-specific T cell receptors (TcR) that are clonally segregated (i.e., one cell lineage-one receptor specificity). Every mature T cell also expresses the CD3 molecule, which is associated with the TcR. In addition mature T cells display one of two accessory molecules, CD4 or CD8. The TcR/CD3 complex recognizes antigens associated with the major histocompatibility complex (MHC) molecules on target cells (e.g. virus-infected cell). The TcR is a transmembrane heterodimer composed of two polypeptide chains (usually, α and β chains). Each chain consists of a constant (C) and a variable (V) region, and are formed by a gene-sorting mechanism similar to that found in antibody formation. The repertoire is generated by combinatorial joining of variable (V), joining (J), and diversity (D) genes, and by N region (nucleotides inserted by the enzyme deoxynucleotidyl-transferase) diversification. Unlike immunoglobulin genes, genes encoding TcR do not undergo somatic mutation. Thus there is no change in the affinity of the TcR during activation, differentiation, and expansion.