T-cells are originally formed from stem cells in the bone marrow, however, T-cells, unlike B-cells, mature in the thymus. The thymus is a lymphoid organ located in the upper chest.

In contrast, B-cells are formed and mature in the bone marrow.

This question asks which of the following is NOT an antigen presenting cell, therefore, any option that is an antigen presenting cell in the immune system is an INCORRECT answer.

During an immune response, the cells involved in antigen presentation are dendritic cells, macrophages, and B-cells. T-cells, then, must be the answer choice that is NOT an antigen presenting cell, and thus is the correct answer.

Neutrophils are professional phagocytes of the immune system. They prevent infection by phagocytosing potential invaders.

Note, however, that neutrophils could not have been the initial cell type to phagocytose a free-living prokaryote. Neutrophils are eukaryotic, and evolved long after endosymbiosis first occurred. They are, however, still closely linked to phagocytosis in humans.

Cell-mediated immunity involves the response of specific cells toward an invading pathogen or organism. This is in contrast to humoral, or antibody-mediated immunity. Both of these are types of adaptive immunity, however, cell-mediated immunity involves the initial identificaiton of an unknown pathogen, while humoral immunity requires prior exposure to the antigen.

B-cells secrete antibodies and are the main actor in humoral immunity; they do not participate directly in cell-mediated immunity. Cytotoxic T-cells are activated by helper T-cells to recognize and destroy infected cells in the body. The process also involves cytokines which recruit neutrophils to digest the infected cell or microbes.

Antigen-presenting cells do all of these functions, thus working to stimulate an adaptive response in regional lymph nodes.

Histocompatibility complex molecules, or MHCs, are keys for carrying antigens and developing antibodies. Once antigen-presenting cells encounter an antigen, they will bind it and carry it to the lymph nodes to activate the adaptive immune response, or to establish cellular memory of a new foreign antigen.

T-cells and B-cells are derived from stem cells that originate in the bone marrow. B-cells continue to mature in the bone marrow; however, T-cells mature in the thymus. Once they are mature, they travel through the blood and reside in the lymph.

Cell-mediated immunity involves all of the differentiated forms of T-lymphocytes. Cytotoxic T-cells (also called killer T-cells) are antigen-specific, and responsible for the destruction of infected cells bearing the given antigen.

Plasma cells and B-cells are part of humoral (antibody) immunity, while neutrophils play an important role in the innate immune response.

When an antigen is presented to a B-cell, it can develop the ability to produce antibodies against that specific antigen. Once the B-cell gains this ability, it is a plasma cell.

T-cells, B-cells, and dendritic cells are derived from lymphoid progenitor stem cells. Together, the group of cells derived from this cell type is known as the lymphocytes. Mast cells, erythrocytes, and monocytes are derived from myeloid progenitor stem cells. Macrophages are derived from monocytes.

Blood cells can be broken into two main categories based on their originating stem cells. Myeloid progenitor cells are the source of erythrocytes and most granulocytes. Lymphoid progenitor cells give rise to lymphocytes.

Lymphocytes are mostly involved in the adaptive immune response, and include dendritic cells, T-cells, B-cells, and the derivatives of these cells, such as plasma cells and memory cells. Natural killer cells, however, are granulocytes that are involved in the innate immune response, but are still derived from lymphoid progenitor cells. Natural killer cells are thus lymphocytes as well.

Neutrophils are granulocytes involved in the innate immune response, and are generated from myeloid progenitor cells; neutrophils are not lymphocytes.

The thymus is responsible for the maturation of T-cells. The thymus, a gland centered in the chest, allows T-cells to be tested against a "self-antigen." If the T-cell does not react against the self-antigen, it is allowed to leave the thymus and enter into circulation to detect foreign antigens. If the T-cell does react to the self-antigen, it is generally destroyed. Failure to destroy these T-cells can result in autoimmune attacks. Upon detection of foreign antigens, mature T-cells differentiate into a variety of other T-cell types and stimulate B-cells to produce antibodies.