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In particular, the following system of ordinary differential equations is considered \\begin{align*} \\begin{split} \\dot C&=\\rho_C(L+B)C+\\rho_C\\beta IC-\\frac{1}{\\tau_C}C,\\\\ \\dot L&=\\rho_LL-\\alpha LC,\\\\ \\dot B&=\\frac{1}{\\tau_I}I -\\alpha BC-\\frac{1}{\\tau_B}B, \\\\ \\dot P&=\\rho_P(2a_Ps(P,I)-1)P-\\frac{1}{\\tau_P}P,\\\\ \\dot I&=\\rho_I(2a_Is(P,I)-1)I-\\frac{1}{\\tau_I}I +\\frac{1}{\\tau_P}P-\\alpha\\beta IC, \\end{split} \\end{align*} where \\(C, L,B,P,I\\) are the number of CAR T cells, leukaemic cells, mature healthy B cells, CD19- haematopoietic stem cells and CD19+ B cell progenitors. The signaling function \\(s\\) is of the form \\(s(P,I) = \\frac{1}{1 + k_s ( P + I ) }\\). The first equation describes the proliferation of CAR T cells due to encounters with their target cells and the second equation the proliferation of leukaemic cells and their death due to encounters with CAR T cells. The remaining three equations describe the evolution of B cells which consist of three compartments.  Assuming a steady state approximation for \\(I\\) and neglecting the contribution of the haematopoietic compartments, the system is reduced to the simplified model \\begin{align*} \\begin{split} \\dot C&=\\rho_C(L+B)C-\\frac{1}{\\tau_C}C,\\\\ \\dot L&=\\rho_LL-\\alpha LC,\\\\ \\dot B&= -\\alpha BC-\\frac{1}{\\tau_B}B. \\end{split} \\end{align*} The dynamics of the reduced system is studied in numerical simulations. In particular, it is shown that the model can explain early post-injection dynamics of the different compartments and the fact that the number of injected CAR T cells does not critically affect the treatment outcome. 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