Transition-metal doping leads to dramatic structural changes and results in novel bonding patterns in small boron clusters. Based on the experimentally derived mono-ring planar C_9v Ta©B₉²⁻ (1) and extensive first-principles theory calculations, we present herein the possibility of high-symmetry double-ring tubular D_9d Ta@B₁₈³⁻ (2) and C_9v Ta₂@B₁₈ (3) and triple-ring tubular D_9h Ta₂@B₂₇⁺ (4), which may serve as embryos of single-walled metalloboronanotube α-Ta₃@B_48(3,0) (5) wrapped up from the recently observed most stable free-standing boron α-sheet on a Ag(111) substrate with a transition-metal wire (–Ta–Ta–) coordinated inside. Detailed bonding analyses indicate that, with an effective d_z²–d_z² overlap on the Ta–Ta dimer along the C₉ molecular axis, both Ta₂@B₁₈ (3) and Ta₂@B₂₇⁺ (4) follow the universal bonding pattern of σ + π double delocalization with each Ta center conforming to the 18-electron rule, providing tubular aromaticity to these Ta-doped boron complexes with magnetically induced ring currents. The IR, Raman, and UV-vis spectra of 3 and 4 are computationally simulated to facilitate their future experimental characterization.