A kidney-transplant patient experienced a cytotoxic rejection of the new kidney. Place the following in order for that rejection:
(1) apoptosis occurs
(2) CD8⁺ T cell becomes CTL
(3) granzymes released
(4) MHC class I activates CD8⁺ T cell
(5) perforin released
a. 1, 2, 3, 4, 5
b. 5, 4, 3, 2, 1
c. 4, 2, 5, 3, 1
d. 3, 4, 5, 1, 2
e. 2, 3, 4, 1, 5

검증된 단계별 안내

Step 1: Understand that cytotoxic rejection involves CD8⁺ T cells recognizing the transplanted kidney cells as foreign through MHC class I molecules presenting antigen. This recognition activates the CD8⁺ T cell.

Step 2: Once activated by MHC class I, the CD8⁺ T cell differentiates into a cytotoxic T lymphocyte (CTL), which is capable of killing target cells.

Step 3: The CTL then releases perforin, a protein that forms pores in the target cell membrane, allowing entry of other molecules.

Step 4: Following perforin pore formation, granzymes are released into the target cell through these pores; granzymes are serine proteases that trigger apoptosis inside the target cell.

Step 5: Finally, apoptosis occurs in the target kidney cells, leading to cell death and contributing to the rejection of the transplanted organ.

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주요 개념

질문에 올바르게 답하기 위해 반드시 이해해야 하는 핵심 개념들은 다음과 같습니다.

Activation of CD8⁺ T Cells by MHC Class I

Cytotoxic T lymphocytes (CTLs) are activated when their T cell receptors recognize antigenic peptides presented by MHC class I molecules on target cells. This activation is the initial step that triggers the CD8⁺ T cell to differentiate into an effector CTL capable of killing infected or foreign cells.

Mechanism of Target Cell Killing by CTLs

Activated CTLs kill target cells by releasing cytotoxic molecules such as perforin and granzymes. Perforin forms pores in the target cell membrane, allowing granzymes to enter and induce apoptosis, effectively eliminating the harmful or foreign cells.

Apoptosis Induction in Cytotoxic Rejection

Apoptosis is a programmed cell death process triggered in target cells by granzymes delivered through perforin pores. This controlled cell death prevents inflammation and tissue damage, playing a key role in cytotoxic rejection during organ transplantation.